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Article

Synthesis of Regiospecifically Fluorinated Conjugated Dienamides

by
Mohammad Chowdhury
,
Samir K. Mandal
,
Shaibal Banerjee
and
Barbara Zajc
*
Department of Chemistry, The City College and The City University of New York, 160 Convent Avenue, NY 10031, USA
*
Author to whom correspondence should be addressed.
Molecules 2014, 19(4), 4418-4432; https://doi.org/10.3390/molecules19044418
Submission received: 16 February 2014 / Revised: 22 March 2014 / Accepted: 31 March 2014 / Published: 10 April 2014
(This article belongs to the Special Issue Fluorine Chemistry 2016)
Browse Figures
Versions Notes

Abstract

:
Modular synthesis of regiospecifically fluorinated 2,4-diene Weinreb amides, with defined stereochemistry at both double bonds, was achieved via two sequential Julia-Kocienski olefinations. In the first step, a Z-α-fluorovinyl Weinreb amide unit with a benzothiazolylsulfanyl substituent at the allylic position was assembled. This was achieved via condensation of two primary building blocks, namely 2-(benzo[d]thiazol-2-ylsulfonyl)-2-fluoro-N-methoxy-N-methylacetamide (a Julia-Kocienski olefination reagent) and 2-(benzo[d]thiazol-2-ylthio)acetaldehyde (a bifunctional building block). This condensation was highly Z-selective and proceeded in a good 76% yield. Oxidation of benzothiazolylsulfanyl moiety furnished a second-generation Julia-Kocienski olefination reagent, which was used for the introduction of the second olefinic linkage via DBU-mediated condensations with aldehydes, to give (2Z,4E/Z)-dienamides in 50%–74% yield. Although olefinations were 4Z-selective, (2Z,4E/Z)-2-fluoro-2,4-dienamides could be readily isomerized to the corresponding 5-substituted (2Z,4E)-2-fluoro-N-methoxy-N-methylpenta-2,4-dienamides in the presence of catalytic iodine.

Graphical Abstract

1. Introduction

The conjugated diene and polyene amide structural units are found in many naturally occurring compounds that possess biological activity [1]. These compounds have a variety of uses, ranging from medicinal purposes, to insecticides, as well as culinary flavoring agents [1]. Some examples of dienamides are shown in Figure 1. Trichostatin A is an antifungal antibiotic [2], and as an inhibitor of mammalian histone deacetylase [3], is a potential anticancer agent [4]. Pellitorine has insecticidal [5] and cytotoxic [6] activities. Piperlonguminine has broad-ranging therapeutic activities [7] such as antibacterial, antifungal, antitumor [8], anticoagulant [9], antimelanogenesis [10], and anti-inflammatory [11], to name a few. Piperovatine exhibits local anesthetic [12] and antinflammatory activities [11]. Due to their interesting biological activities, several analogs, such as a fluorinated Trichostatin A analog [13], have been synthesized as well.
Molecules 19 04418 g001 550
Figure 1. Examples of naturally occurring, biologically active 2,4-dienamides.
Figure 1. Examples of naturally occurring, biologically active 2,4-dienamides.
Molecules 19 04418 g001
Fluorine is an attractive substituent in pharmaceuticals, in agrochemicals, and in materials chemistry [14,15,16] due to its effect on physical, chemical, and biological properties of compounds [17,18,19]. Julia-Kocienski olefinations [20,21,22,23] have been explored for the synthesis of various functionalized fluoroolefins [24,25,26] by us [27,28,29,30,31,32,33,34,35] and by others [36,37,38,39,40,41,42,43,44,45,46]. In the course of our recent work, we became interested in the use of bifunctional Julia-Kocienski reagents, or their precursors, for novel modular assembly of vinyl [33,47] and fluorovinyl [33] compounds. Herein, we report the synthesis of regiospecifically fluorinated dienamides, via sequential olefination of a bifunctional Julia-Kocienski building block. As the amide functionality, we chose the Weinreb amide, both to test the feasibility of the methodology and due to its versatility via its unique reactivity properties [48,49,50,51].

2. Results and Discussion

Key to our approach was the assembly of a α-fluorovinyl Weinreb amide moiety with functionality at the beta position that could be used in a sequential condensation. We have previously reported the synthesis and studied the reactivity of a Julia-Kocienski reagent for the preparation of α-fluorovinyl Weinreb amides (1, Scheme 1) [31]. Condensation of 2-(benzo[d]thiazol-2-ylsulfonyl)-2-fluoro-N-methoxy-N-methylacetamide (1) with a 2-(heteroarylthio)ethanal (2, heteroaryl = benzothiazolyl, Scheme 1) and subsequent oxidation would furnish a second-generation Julia-Kocienski reagent for dienamide synthesis. A retrosynthetic approach to conjugated dieneamides is outlined in Scheme 1.
Molecules 19 04418 g002 550
Scheme 1. Retrosynthetic analysis for the preparation of conjugated dieneamides.
Scheme 1. Retrosynthetic analysis for the preparation of conjugated dieneamides.
Molecules 19 04418 g002
The requisite Julia-Kocienski reagent, 2-(benzo[d]thiazol-2-ylsulfonyl)-2-fluoro-N-methoxy-N-methylacetamide (1), was synthesized as reported [31]. Synthesis of the other key reactive partner, 2-(benzo[d]thiazol-2-ylthio)acetaldehyde (2), was initially attempted via the dioxolane derivative of 2. Although the dioxolane derivative of 2 could be readily prepared from 2-(bromomethyl)-1,3-dioxolane and the sodium salt of 2-mercapto-1,3-benzothiazole, attempts at deprotection of 2-[(1,3-dioxolan-2-yl)methylthio]benzo[d]thiazole under various conditions proved unsuccessful. Therefore, synthesis via the dimethyl acetal was considered (Scheme above Table 1).
Table
Table 1. Synthesis of 2-(benzo[d]thiazol-2-ylthio)acetaldehyde 2. Molecules 19 04418 i001
Table 1. Synthesis of 2-(benzo[d]thiazol-2-ylthio)acetaldehyde 2. Molecules 19 04418 i001
EntryReagentSolventT (°C)TimeYield (%) a
1I2acetonertovernight-- b
2CBr4CH3CN–H2O 1:3803 days-- b
3PTSATHF–H2O 1:1rt3 days-- b
4HCl (4 M)acetone4024 h20 c
5HCl (4 M)acetone404 h56
6HCl (12 M)acetone5030 min81
7HCl (12 M)acetone–H2O 10:15040 min84
a Aldehyde 2 was unstable under chromatographic conditions, either on silica gel or on alumina. Therefore, the yield reported for 2 is without purification, unless stated otherwise; b 1H-NMR and TLC showed only dimethyl acetal 3, and no product formation was observed; c Isolated yield after column chromatography.
Various conditions were tested to unmask the aldehyde functionality (Table 1). Upon reaction of dimethyl acetal 3 with I2 (entry 1), CBr4 (entry 2), or PTSA (entry 3), no hydrolysis was observed. Reaction of 3 with 4 M HCl at 40 °C resulted in complete consumption of 3, but aldehyde 2 was isolated in a low 20% yield after column chromatography (entry 4). Subsequently, we found that compound 2 is unstable under chromatography conditions, on silica gel and alumina [52]. The yield of crude 2 after hydrolysis with 4 M HCl, but without chromatography, was 56%. Hydrolysis with 12 M HCl at 50 °C was complete within 30 min, yielding crude 2 in 81% yield (entry 6). However, due to the solubility of 2 in water, we obtained inconsistent results in repeat experiments. After extensive experimentation we found that crude 2 could be isolated in consistent yields when aqueous workup was avoided. Briefly, acetal 3 was reacted with 12 M HCl in acetone–H2O (10:1) at 50 °C for 40 min (entry 7), solid NaHCO3 was added portion-wise at 5 °C to neutralize the acid, and excess water was removed by addition of anhydrous Na2SO4. The solution was then passed through a bed of anhydrous Na2SO4 and the solvent was evaporated to afford 2 in >80% yield. When acetone alone was used as solvent, complete hydrolysis of 3 occurred, but the crude product showed the presence of an unidentified byproduct that could possibly result from the condensation of acetone and 2. The use of water as a co-solvent therefore seems to be crucial in order to minimize the formation of the byproduct.
With both desired building blocks in hand, i.e., the Julia-Kocienski reagent 1 and aldehyde 2, we tested reaction conditions for the olefination reaction (Table 2). All condensation reactions were performed at −78 °C in the presence of LHMDS, and gave (Z)-4-(benzo[d]thiazol-2-ylthio)-2-fluoro-N-methoxy-N-methylbut-2-enamide (4) as the only stereoisomer. Comparably, exclusive Z-selectivity has also been observed in NaH-mediated condensations of 1 with aldehydes [31]. In the reactions herein, the molar ratio of sulfone 1, aldehyde 2, and LHMDS was critical for obtaining a good yield of 4 (Table 2). When aldehyde 2 was used as a limiting reactant (entry 1), or in an equimolar amount (entry 2), enamide 4 was obtained in low yield. On the other hand, with excess aldehyde 2 and LHMDS, a substantial yield improvement was observed. Thus, product 4 was isolated in 76% yield when 2 molar equiv of 2 and 3 molar equiv of LHMDS were used (entry 4). Since the desired product was obtained with exclusive Z-selectivity and in a good yield, we did not attempt to use other bases, such as KHMDS or NaHMDS.
Table
Table 2. Synthesis of (Z)-4-(benzo[d]thiazol-2-ylthio)-2-fluoro-N-methoxy-N-methylbut-2-enamide (4). Molecules 19 04418 i002
Table 2. Synthesis of (Z)-4-(benzo[d]thiazol-2-ylthio)-2-fluoro-N-methoxy-N-methylbut-2-enamide (4). Molecules 19 04418 i002
EntryMolar Ratio of 1:2:LHMDSTimeYield (%) a
11.5:1:1.53 h32
21:1:22.5 h20
31:3:54 h60
41:2:33.5 h76
a Yield is of isolated and purified product 4. Reactions were monitored for completion by 19F-NMR. LHMDS was added portion-wise (please see Experimental Section).
In order to obtain the second generation Julia-Kocienski reagent 5, sulfide 4 was oxidized using H5IO6 and catalytic CrO3. Sulfone 5, obtained in 63% yield, was then used for the screening of reaction conditions for the olefination with 2-naphthaldehyde (Table 3).
Table
Table 3. Conditions tested for olefination reactions using the second generation Julia-Kocienski reagent 5 and 2-naphthaldehyde. Molecules 19 04418 i003
Table 3. Conditions tested for olefination reactions using the second generation Julia-Kocienski reagent 5 and 2-naphthaldehyde. Molecules 19 04418 i003
EntryBaseSolventTTime% 4E/4Z Ratio aYield (%) b
1LHMDSTHF−78 to 0 °Covernight---- c
2LHMDSTHF0 °C to rt12 h---- c
3DBUTHFrt2 h---- c
4DBUTHF−78 to 0 °Covernight57/4335
5Cs2CO3THF0 °Covernight---- c
6DBUTHF0 °Covernight43/5755
7Cs2CO3CH2Cl20 °Covernight---- c
8DBUCH2Cl20 °Covernight35/6566
a The relative ratio of isomers in the crude reaction mixtures was determined by 19F-NMR prior to isolation. No change in the relative ratio was observed after purification; b Yield is of isolated and purified product 6a; c No product was detected either by 19F-NMR or by TLC.
Both selectivity and product yield depended upon the reaction conditions. No product formation occurred when LHMDS was used as base (entries 1 and 2), or with DBU as base in THF at room temperature (entry 3). Similarly, Cs2CO3 in either THF or CH2Cl2 at 0 °C did not show product formation (entries 5 and 7). Product 6a was obtained in a low 35% yield and with a moderate 4E selectivity in an overnight reaction with DBU in THF, at −78 to 0 °C (E/Z 57/43, entry 4). When the condensation reaction was allowed to run overnight at 0 °C (entry 6), product 6a was isolated in a better 55% yield, but with a reversed selectivity as compared to entry 4 (E/Z 43/57). Yield and selectivity increased when the condensation reaction was performed overnight using DBU as base in CH2Cl2, at 0 °C (66%, entry 8).
Using these conditions, the generality of condensation reactions of Julia-Kocienski reagent 5 with other aldehydes was tested. Table 4 shows yields, the 4E/4Z ratios, and 19F-NMR data of the products.
Table
Table 4. Reactions of reagent 5 with aldehydes: yields, E/Z ratios, and 19F-NMR data. Molecules 19 04418 i004
Table 4. Reactions of reagent 5 with aldehydes: yields, E/Z ratios, and 19F-NMR data. Molecules 19 04418 i004
EntryRCHOProduct (6a–e);
% 4E/4Z Ratio a; Yield (%) b		19F-NMR Data: c
δ (ppm); Mult, J (Hz)
1 Molecules 19 04418 i0066a: 35/65; 66(4E)-6a: −123.4; d, 30.5
(4Z)-6a: −121.2; d, 30.5
2 Molecules 19 04418 i0076b: 23/77; 50(4E)-6b: −125.2; d, 33.6
(4Z)-6b: −122.6; d, 33.6
3 Molecules 19 04418 i0086c: 40/60; 74(4E)-6c: −119.6; d, 30.5
(4Z)-6c: −118.4; d, 30.5
4 Molecules 19 04418 i0096d: 10/90; 63(4E)-6d: −123.7; d, 30.5
(4Z)-6d: −120.7; d, 33.6
5 Molecules 19 04418 i0106e: 15/85; 51(4E)-6e: −125.7; d, 30.5
(4Z)-6e: −124.2; d, 33.6
a The relative ratio of isomers in the crude reaction mixtures was determined by 19F-NMR prior to isolation; b Yield is of isolated and purified product 6; c 19F-NMR spectra were recorded at 282 MHz, in CDCl3 with CFCl3 as an internal reference.
Moderate to high 4Z selectivity was obtained with electron-rich aryl and heteroaryl aldehydes, with yields ranging from 50%–66% (entries 1, 2 and 4). The electron-deficient p-nitrobenzaldehyde gave product 6c in a good 74% yield, but with poor 4Z selectivity (entry 3). Reaction of 5 with 3-phenylpropanal gave product 6e in a moderate 51% yield and with high 4Z selectivity (entry 5). In the 19F-NMR spectra of all products, the doublet from the (4E)-isomer appears more upfield as compared to the doublet from the (4Z)-isomer (Table 4, entries 1–5).
Next, we considered isomerization of the (2Z,4Z)-isomer to the (2Z,4E)-isomer. Several techniques were evaluated to effect this isomerization. Overnight exposure of the 4E/4Z isomer mixture to light (20 watt bulb) did not cause any isomerization. Treatment of the isomer mixtures with silica powder in CHCl3 at room temperature or at 0 °C showed the desired isomerization, but the isomerization did not proceed to completion. A convenient method for the isomerization using catalytic I2 in CHCl3 at room temperature has been reported [53]. Using this method, complete isomerization of (2Z,4E/Z)-6a–d to (2Z,4E)-6a–d was achieved (Table 5).
Table
Table 5. Isomerization of (2Z,4E/Z)-6a–d to (2Z,4E)-6a–d. Molecules 19 04418 i005
Table 5. Isomerization of (2Z,4E/Z)-6a–d to (2Z,4E)-6a–d. Molecules 19 04418 i005
EntryIsomer MixtureTimeProduct aYield (%) b
1(2Z,4E/Z)-6a3 h(2Z,4E)-6a75
2(2Z,4E/Z)-6b3 h(2Z,4E)-6b86
3(2Z,4E/Z)-6c1.5 h(2Z,4E)-6c89
4(2Z,4E/Z)-6dovernight(2Z,4E)-6d92
a Olefin geometry was determined by 1H-NMR; b Yield is of the isolated and purified isomer.

3. Experimental

3.1. General Information

THF was distilled over LiAlH4 and then over sodium. CH2Cl2, EtOAc, and hexanes were distilled over CaCl2. For reactions performed under a nitrogen atmosphere, glassware was dried with a heat gun under vacuum. LHMDS (1.0 M in THF) was obtained from commercial sources. Julia Kocienski reagent 2-(benzo[d]thiazol-2-ylsulfonyl)-2-fluoro-N-methoxy-N-methylacetamide (1) was prepared from the known 2-(benzo[d]thiazol-2-ylsulfonyl)-N-methoxy-N-methylacetamide [54], via metalation-fluorination using our previously reported procedure [31]. All other reagents were obtained from commercial sources and used without further purification. Thin layer chromatography was performed on Analtech silica gel plates (250 μm). Column chromatographic purifications were performed on 200–300 mesh silica gel. 1H-NMR spectra were recorded at 500 MHz in CDCl3 and are referenced to residual solvent. 13C-NMR spectra were recorded at 125 MHz and are referenced to the carbon resonance of the deuterated solvent. 19F-NMR spectra were recorded at 282 MHz with CFCl3 as an internal standard. Chemical shifts (δ) are reported in parts per million and coupling constants (J) are in hertz (Hz).

3.2. Synthesis of “Second-Generation” Julia-Kocienski Reagent 5

2-(2,2-Dimethoxyethylthio)benzo[d]thiazole 3. To a solution of the sodium salt of 2-mercapto-1,3-benzothiazole (1.67 g, 8.83 mmol, 1.49 molar equiv.) in DMF (20 mL) was added 2-bromo-1,1-dimethoxyethane (1.00 g, 5.91 mmol), and the mixture was allowed to stir at 40 °C for 4 h. Upon completion of the reaction, as observed by TLC, the reaction mixture was diluted with EtOAc and washed with water. The aqueous layer was extracted with EtOAc (3 × 30 mL). The combined organic layer was washed with saturated NaHCO3 (30 mL), brine, dried over anhydrous Na2SO4, and evaporated. The crude product was purified by column chromatography using 20% EtOAc in hexanes to obtain compound 3 (0.769 g, 51%) as a colorless viscous liquid. Rf (SiO2, 20% EtOAc in hexanes): 0.48. 1H-NMR (CDCl3): δ 7.85 (d, 1H, Ar-H, J = 7.8 Hz), 7.75 (d, 1H, Ar-H, J = 8.3 Hz), 7.41 (t, 1H, Ar-H, J = 7.8 Hz), 7.29 (t, 1H, Ar-H, J = 7.8 Hz), 4.72 (t, 1H, J = 5.3 Hz), 3.58 (d, 2H, J = 5.3 Hz), 3.44 (s, 6H, OCH3). 13C-NMR (CDCl3): δ 166.4, 153.2, 135.5, 126.1, 124.4, 121.6, 121.1, 103.0, 54.3, 35.5. HRMS (ESI) calcd for C11H14NO2S2 [M+H]+ 256.0460, found 256.0462.
2-(Benzo[d]thiazol-2-ylthio)acetaldehyde 2. To a stirred solution of 2-(2,2-dimethoxyethylthio)benzo[d]thiazole (3, 1.60 g, 6.26 mmol) in acetone (48 mL), was slowly added a mixture of HCl (12 M, 10.6 mL) and water (5.2 mL) at rt. The mixture was stirred for 40 min at 50 °C. Upon completion of the reaction, as observed by TLC, the mixture was cooled to 5 °C and the reaction was quenched by portion-wise addition of solid NaHCO3 up to the neutralization point, and then passed through a bed of anhydrous Na2SO4. The anhydrous Na2SO4 bed was washed with a minimum amount of acetone, the combined eluent was dried over anhydrous Na2SO4, and concentrated under reduced pressure. Crude product 2 (1.10 g, 84%) was used in the next step without purification. Rf (SiO2, 20% EtOAc in hexanes): 0.29. 1H-NMR (CDCl3): δ 9.73 (br, 1H), 7.85 (d, 1H, Ar-H, J = 7.9 Hz), 7.76 (d, 1H, Ar-H, J = 8.2 Hz), 7.42 (t, 1H, Ar-H, J = 7.6 Hz), 7.32 (t, 1H, Ar-H, J = 7.6 Hz), 4.09 (d, 2H, J = 1.8 Hz).
(Z)-4-(Benzo[d]thiazol-2-ylthio)-2-fluoro-N-methoxy-N-methylbut-2-enamide 4. To a stirred solution of 2-(benzo[d]thiazol-2-ylsulfonyl)-2-fluoro-N-methoxy-N-methylacetamide (1, 0.700 g, 2.20 mmol) and 2-(benzo[d]thiazol-2-ylthio)acetaldehyde (2, 0.930 g, 4.44 mmol, 2.0 molar equiv.) in dry THF (48.0 mL) at −78 °C (dry ice/iPrOH), was added LHMDS (4.39 mL, 1 M, 4.39 mmol, 2.0 molar equiv.) dropwise under a nitrogen atmosphere. The mixture was allowed to stir at −78 °C (dry ice/iPrOH) for 2 h and checked for the disappearance of 1 by 19F-NMR (a small sample was removed by syringe and checked by NMR). Since 19F-NMR showed the presence of 1, more LHMDS (2.19 mL, 1 M, 2.19 mmol, 1 molar equiv.) was added and the mixture was allowed to stir at −78 °C for an additional 1 h at which time complete consumption of sulfone 1 was observed by 19F-NMR. The reaction was quenched by the addition of saturated aq. NH4Cl, the solvent was partially removed under reduced pressure, and the mixture was extracted with EtOAc (3×). The combined organic layer was washed with 5% aq. NaOH, followed by water and brine, and then dried over Na2SO4. The organic layer was concentrated under reduced pressure and the crude product was purified by column chromatography using 10%, 15%, and 20% EtOAc in hexanes, to afford compound 4 as a yellow wax (0.523 g, 76%). Rf (SiO2, 30% EtOAc in hexanes): 0.54. 1H-NMR (CDCl3): δ 7.87 (d, 1H, Ar-H, J = 8.3 Hz), 7.75 (d, 1H, Ar-H, J = 7.8 Hz), 7.43–7.40 (m, 1H, Ar-H), 7.32–7.28 (m, 1H, Ar-H), 6.22 (dt, 1H, J = 32.7; 8.0 Hz), 4.15 (dd, 2H, J = 8.0; 1.5 Hz), 3.69 (s, 3H, OCH3), 3.22 (s, 3H, CH3). 13C-NMR (CDCl3): δ 165.2, 161.8 (d, JCF = 27.9 Hz), 153.3, 152.4 (d, JCF = 271.9 Hz), 135.7, 126.3, 124.6, 121.9, 121.2, 113.0 (d, JCF = 10.5 Hz), 62.1, 33.9, 26.9 (d, JCF = 5.5 Hz). 19F-NMR (CDCl3): δ −119.9 (d, 3JHF = 30.5 Hz). HRMS (ESI) calcd for C13H14FN2O2S2 [M+H]+ 313.0475, found 313.0480.
(Z)-4-(Benzo[d]thiazol-2-ylsulfonyl)-2-fluoro-N-methoxy-N-methylbut-2-enamide 5. H5IO6 (0.477 g, 2.09 mmol, 3.0 molar equiv) was dissolved in CH3CN (80.0 mL) by vigorous stirring at rt for 20 min. CrO3 (25.0 mg, 0.25 mmol) was added and the reaction mixture was stirred for an additional 5 min to give an orange-colored solution. A solution of (Z)-4-(benzo[d]thiazol-2-ylthio)-2-fluoro-N-methoxy-N-methybut-2-enamide (4, 0.218 g, 0.698 mmol) in CH3CN (10.0 mL) was added dropwise to this mixture, resulting in an exothermic reaction and the formation of a yellowish precipitate. After complete addition, the mixture was stirred for 3 h, at which time TLC showed complete consumption of amide 4. The mixture was filtered through a Celite pad, the pad was washed with CH3CN, and the filtrate was concentrated under reduced pressure. Water was added to the residue and the mixture was extracted with EtOAc (3 × 30 mL). The combined organic layer was washed with saturated aq. NaHCO3 (5 × 30 mL) and brine (30 mL), and dried over anhydrous Na2SO4. The organic layer was concentrated under reduced pressure and the crude product was purified by column chromatography using 15%, 20%, and 25% EtOAc in hexanes to afford compound 5 as a white solid (0.152 g, 63%). Rf (SiO2, 40% EtOAc in hexanes): 0.43. 1H-NMR (CDCl3): δ 8.24 (d, 1H, Ar-H, J = 7.8 Hz), 8.02 (d, 1H, Ar-H, J = 7.8 Hz), 7.67–7.59 (m, 2H, Ar-H), 5.96 (dt, 1H, J = 31.2; 8.3 Hz), 4.43 (dd, 2H, J = 8.3; 1.5 Hz), 3.53 (s, 3H, OCH3), 3.17 (s, 3H, CH3). 13C-NMR (CDCl3): δ 164.8, 160.8 (d, JCF = 28.4 Hz), 155.6 (d, JCF = 279.7 Hz), 152.8, 137.2, 128.4, 127.9, 125.8, 122.6, 102.7 (d, JCF = 10.1 Hz), 62.1, 51.1 (d, JCF = 4.6 Hz), 33.6. 19F-NMR (CDCl3): δ −113.6 (d, 3JHF = 30.5 Hz). HRMS (ESI) calcd for C13H14FN2O4S2 [M+H]+ 345.0374, found 345.0376.

3.3. Condensation Reactions of Julia-Kocienski Reagent 5

General experimental procedure. To a stirred solution of aldehyde (0.20 mmol) in dry CH2Cl2 (10.0 mL) was added DBU (121.7 mg, 0.80 mmol, 4.0 molar equiv.) and the mixture was cooled to 0 °C. A solution of (Z)-4-(benzo[d]thiazol-2-ylsulfonyl)-2-fluoro-N-methoxy-N-methylbut-2-enamide (5, 103.3 mg, 0.300 mmol, 1.5 equiv.) in dry CH2Cl2 (10.0 mL) was then added slowly, dropwise (over about 2 h). The reaction mixture was allowed to stir overnight at 0 °C. After completion of the reaction, the solvent was evaporated under a stream of nitrogen gas, and the 1H and 19F-NMR spectra of the crude product mixture were recorded for determination of the E/Z ratio. The combined E/Z product mixture was purified by column chromatography. For eluting solvents see the specific compound headings. The mixture of (4E)- and (4Z)-isomers was analyzed and characterized based on the 1H-NMR; the assignment and integration of specific olefinic proton(s) allowed for other signals to be assigned based on the integration, along with a comparison to the pure (2Z,4E)-isomer (obtained after isomerization, vide infra). Assignment of the 19F-NMR signals to the (4E)- and (4Z)-isomers was based on the integration.
(2Z,4E/Z)-2-Fluoro-N-methoxy-N-methyl-5-(naphthalen-2-yl)penta-2,4-dienamide 6a. Isomer ratio of (4E)-6a:(4Z)-6a = 35:65. Column chromatography using 8%, 10%, and 15% EtOAc in hexanes gave a mixture of (2Z,4E/Z)-6a as a white solid (38.0 mg, 66%). Rf (SiO2, 30% EtOAc in hexanes): 0.49 for (4E)-6a and 0.58 for (4Z)-6a. 1H-NMR (CDCl3): δ 7.85–7.80 (m, Ar-H, 4H, (4E)-isomer and 4H, (4Z)-isomer), 7.68 (dd, 1H, Ar-H, J = 8.3; 1.5 Hz, (4E)-isomer), 7.50–7.45 (m, Ar-H, 2H, (4E)-isomer and 3H, (4Z)-isomer), 7.21 (dd, 1H, J = 15.6; 11.2 Hz, (4E)-isomer), 7.06 (ddd, 1H, J = 32.7; 12.0; 1.0 Hz, (4Z)-isomer), 6.97 (d, 1H, J = 15.6 Hz, (4E)-isomer), 6.91 (d, 1H, J = 11.2 Hz, (4Z)-isomer), 6.72 (dd, 1H, J = 32.5; 11.5 Hz, (4E)-isomer), 6.66 (t, 1H, J = 11.7 Hz, (4Z)-isomer), 3.80 (s, 3H, OCH3, (4E)-isomer), 3.76 (s, 3H, OCH3, (4Z)-isomer), 3.29 (s, 3H, CH3, (4E)-isomer), 3.25 (s, 3H, CH3, (4Z )isomer). 19F-NMR (CDCl3): δ –121.2 (d, 3JHF = 30.5 Hz, (4Z)-isomer), −123.4 (d, 3JHF = 30.5 Hz, (4E)-isomer). HRMS (ESI) calcd for C17H17FNO2 [M+H]+ 286.1238, found 286.1242.
(2Z,4E/Z)-2-Fluoro-N-methoxy-N-methyl-5-(4-methoxyphenyl)penta-2,4-dienamide 6b. Isomer ratio of (4E)-6b:(4Z)-6b = 23:77. Column chromatography using 8%, 15%, and 20% EtOAc in hexanes gave a mixture of (2Z,4E/Z)-6b as a pale yellow solid (26.5 mg, 50%). Rf (SiO2, 30% EtOAc in hexanes): 0.35. 1H-NMR (CDCl3): δ 7.42 (d, 2H, Ar-H, J = 8.8 Hz, (4E)-isomer), 7.29 (d, 2H, Ar-H, J = 8.8 Hz, (4Z)-isomer), 6.99 (ddd, 1H, J = 32.7; 11.7; 0.9 Hz, (4Z)-isomer), 6.95 (dd, 1H, J = 15.6; 11.2 Hz, (4E)-isomer), 6.91–6.87 (m, Ar-H, 2H, (4Z)-isomer and 2H, (4E)-isomer), 6.75 (d, 1H, J = 15.6 Hz, (4E)-isomer), 6.69 (br d, 1H, J = 11.7 Hz, (4Z)-isomer), 6.65 (dd, 1H, J = 32.7; 11.4 Hz, (4E)-isomer), 6.47 (t, 1H, J = 11.7 Hz, (4Z)-isomer), 3.83 (s, 3H, OCH3, (4E)-isomer), 3.82 (s, 3H, OCH3, (4Z)-isomer), 3.77 (s, 3H, OCH3, (4E)-isomer), 3.76 (s, 3H, OCH3, (4Z)-isomer), 3.27 (s, 3H, CH3, (4E)-isomer), 3.25 (s, 3H, CH3, (4Z)-isomer). 19F-NMR (CDCl3): δ −122.6 (d, 3JHF = 33.6, (4Z)-isomer), −125.2 (d, 3JHF = 33.6, (4E)-isomer). HRMS (ESI) calcd for C14H17FNO3 [M+H]+ 266.1187, found 266.1191.
(2Z,4E/Z)-2-Fluoro-N-methoxy-N-methyl-5-(4-nitrophenyl)penta-2,4-dienamide 6c. Isomer ratio of (4E)-6c:(4Z)-6c = 4:6. Column chromatography using 10% and 15% EtOAc in hexanes gave a mixture of (2Z,4E/Z)-6c as a yellow solid (41.3 mg, 74%). Rf (SiO2, 30% EtOAc in hexanes): 0.47 for (4E)-6c and 0.72 for (4Z)-6c. 1H-NMR (CDCl3): δ 8.23 (d, 2H, Ar-H, J = 8.8 Hz, (4Z)-isomer), 8.21 (d, 2H, Ar-H, J = 8.7 Hz, (4E)-isomer), 7.60 (d, 2H, Ar-H, J = 8.8 Hz, (4E)-isomer), 7.48 (d, 2H, Ar-H, J = 8.3 Hz, (4Z)-isomer), 7.23 (dd, 1H, J = 15.9; 11.5 Hz, (4E)-isomer), 6.86–6.61( m, 3H, (4Z)-isomer and 2H, (4E)-isomer), 3.79 (s, 3H, OCH3, (4E)-isomer), 3.77 (s, 3H, OCH3, (4Z)-isomer), 3.28 (s, 3H, CH3, (4E)-isomer), 3.25 (s, 3H, CH3, (4Z)-isomer). 19F-NMR (CDCl3): δ −118.4 (d, 3J HF = 30.5 Hz, (4Z)-isomer), −119.6 (d, 3J HF = 30.5 Hz, (4E)-isomer). HRMS (ESI) calcd for C13H14FN2O4 [M+H]+ 281.0932, found 281.0935.
(2Z,4E/Z)-2-Fluoro-N-methoxy-N-methyl-5-(thiophen-2-yl)penta-2,4-dienamide 6d. Isomer ratio of (4E)-6d:(4Z)-6d = 1:9. Column chromatography using 8% and 10% EtOAc in hexanes gave a mixture of (2Z,4E/Z)-6d as a yellow solid (30.2 mg, 63%). Rf (SiO2, 30% EtOAc in hexanes): 0.34 for (4E)-6d and 0.37 for (4Z)-6d. 1H-NMR (CDCl3): δ 7.36 (d, 1H, Ar-H, J = 4.9 Hz, (4Z)-isomer), 7.27 (ddd, 1H, J = 31.7; 12.2; 1.0 Hz, (4Z)-isomer), 7.27–7.25 (overlapping with CHCl3, 1H, Ar-H, (4E)-isomer), 7.12 (d, 1H, Ar-H, J = 3.4 Hz, (4Z)-isomer), 7.09 (d, 1H, Ar-H, J = 3.4 Hz, (4E)-isomer), 7.04 (dd, 1H, Ar-H, J = 5.1; 3.7 Hz, (4Z)-isomer), 7.00 (dd, 1H, Ar-H, J = 5.1; 3.7 Hz, (4E)-isomer), 6.92 (d, 1H, J = 15.6 Hz, (4E)-isomer), 6.86 (dd, 1H, J = 15.6; 10.7 Hz, (4E)-isomer), 6.76 (br d, 1H, J = 11.2 Hz, (4Z)-isomer), 6.61 (dd, 1H, J = 32.2; 10.7 Hz, (4E)-isomer), 6.42 (t, 1H, J = 12.0 Hz, (4Z)-isomer), 3.78 (s, 3H, OCH3, (4Z)-isomer), 3.77 (s, 3H, OCH3, (4E)-isomer), 3.28 (s, 3H, CH3, (4Z)-isomer), 3.26 (s, 3H, CH3, (4E)-isomer). 19F-NMR (CDCl3): δ −120.7 (d, 3JHF = 33.6 Hz, (4Z)-isomer), −123.7 (d, 3JHF = 30.5 Hz, (4E)-isomer). HRMS (ESI) calcd for C11H13FNO2S [M+H]+ 242.0646, found 242.0647.
(2Z,4E/Z)-2-Fluoro-N-methoxy-N-methyl-7-phenylhepta-2,4-dienamide 6e. Isomer ratio of (4E)-6e:(4Z)-6e = 15:85. Column chromatography using 6%, 8%, and 12% EtOAc in hexanes gave a mixture of (2Z,4E/Z)-6e as a colorless oil (26.6 mg, 51%). Rf (SiO2, 30% EtOAc in hexanes): 0.30. We were unable to resolve the 1H-NMR signals for both isomers, so the signals reported are for the major (2Z,4Z)-isomer. For the minor isomer, only diagnostic vinylic C4-H could be unequivocally assigned (separately listed, vide infra). 1H-NMR (CDCl3) of (2Z,4Z)-isomer: δ 7.30–7.27 (m, 2H, Ar-H), 7.20–7.18 (m, 3H, Ar-H), 6.68 (ddd, 1H, J = 32.7; 11.7; 1.0 Hz), 6.34 (t, 1H, J = 11.2 Hz), 5.80 (dt, 1H, J = 10.7; 7.8 Hz), 3.74 (s, 3H, OCH3), 3.24 (s, 3H, CH3), 2.73 (t, 2H, J = 7.8 Hz), 2.55 (q, 2H, J = 7.8 Hz). Minor (2Z,4E)-isomer (CDCl3): δ 6.04 ppm (1H, C4-H, J = 14.7; 7.3 Hz). 19F-NMR (CDCl3): δ −124.2 (d, 3JHF = 33.6 Hz, (4Z)-isomer), −125.7 (d, 3JHF = 30.5 Hz, (4E)-isomer). HRMS (ESI) calcd for C15H19FNO2 [M+H]+ 264.1394, found 264.1407.

3.4. Isomerization of the (2Z,4E/Z)-Isomer Mixture of 6a–d to the (2Z,4E)-Isomer

General experimental procedure. To a stirred solution of the (2Z,4E/Z)-isomer mixture 6 in dry CHCl3 was added I2 (7–10 mol %) and the mixture was stirred at rt. The reaction was monitored by 19F-NMR and when only one isomer was observed, the reaction mixture was diluted with EtOAc (30 mL). The mixture was washed with water, saturated aq. Na2S2O3 (2 × 10 mL), and dried over Na2SO4. The organic layer was concentrated under reduced pressure to afford the desired (2Z,4E)-isomer. HMQC data were obtained for (2Z,4E)-6c and (2Z,4E)-6d, and where unequivocally assigned, through-bond C–F couplings are reported as 1JCF, 2JCF, etc. Due to the close structural similarity, these couplings are also reported for (2Z,4E)-6a and (2Z,4E)-6b, where possible.
(2Z,4E)-2-Fluoro-N-methoxy-N-methyl-5-(naphthalene-2-yl)penta-2,4-dienamide (2Z,4E)-6a. Isomerization was performed with (2Z,4E/Z)-6a (16.0 mg, 0.056 mmol) in CHCl3 (8.0 mL) using I2 (1.2 mg, 4.7 × 10−3 mmol, 8.4 mol %), in a reaction time of 3 h, to yield isomer (2Z,4E)-6a as a white solid (12.0 mg, 75%). Rf (SiO2, 30% EtOAc in hexanes): 0.49. 1H-NMR (CDCl3): δ 7.83–7.80 (m, 4H, Ar-H), 7.69 (dd, 1H, Ar-H, J = 8.3; 1.5 Hz), 7.50–7.46 (m, 2H, Ar-H), 7.21 (dd, 1H, J = 15.8; 11.3 Hz), 6.97 (d, 1H, J = 15.8 Hz), 6.72 (dd, 1H, J = 32.4; 11.3 Hz), 3.80 (s, 3H, OCH3), 3.29 (s, 3H, CH3). 13C-NMR (CDCl3): δ 162.8 (d, 2JCF = 26.5 Hz), 150.2 (d, 1JCF = 275.6 Hz), 137.9 (d, 4JCF = 4.5 Hz), 134.1 (d, J = 1.9 Hz), 133.7, 128.7, 128.4, 128.0 (d, J = 1.8 Hz), 127.9, 126.8, 126.7, 123.6, 119.6 (d, 3JCF = 3.7 Hz),118.2 (d, 2JCF = 9.2 Hz), 62.1 (d, 5JCF = 2.8 Hz), 34.3. 19F-NMR (CDCl3): δ −123.4 (d, 3JHF = 30.5 Hz).
(2Z,4E)-2-Fluoro-N-methoxy-N-methyl-5-(4-methoxyphenyl)penta-2,4-dienamide (2Z,4E)-6b. Isomerization was performed with (2Z,4E/Z)-6b (14.0 mg, 0.053 mmol) in CHCl3 (8.0 mL) using I2 (1.3 mg, 5.1 × 10−3 mmol, 10 mol %), in a reaction time of 3 h, to yield isomer (2Z,4E)-6b as a pale yellow solid (12.0 mg, 86%). Rf (SiO2, 30% EtOAc in hexanes): 0.35. 1H-NMR (CDCl3): δ 7.42 (d, 2H, Ar-H, J = 7.3 Hz), 6.95 (dd, 1H, J = 15.6; 11.2 Hz), 6.88 (d, 2H, Ar-H, J = 6.8 Hz), 6.75 (d, 1H, J = 15.6 Hz), 6.65 (dd, 1H, J = 32.2; 11.2 Hz), 3.83 (s, 3H, OCH3), 3.77 (s, 3H, OCH3), 3.26 (s, 3H, CH3). 13C-NMR (CDCl3): δ 162.9 (d, 2JCF = 26.8 Hz), 160.4, 149.5 (d, 1JCF = 272.8 Hz), 137.5 (d, 4JCF = 4.3 Hz), 129.5, 128.7, 118.7 (d, 2JCF = 9.1 Hz), 117.2, 114.5, 62.1, 55.6, 34.3. 19F-NMR (CDCl3): δ –125.2 (d, 3JHF = 33.6 Hz).
(2Z,4E)-2-Fluoro-N-methoxy-N-methyl-5-(4-nitrophenyl)penta-2,4-dienamide (2Z,4E)-6c. Isomerization was performed with (2Z,4E/Z)-6c (4.5 mg, 0.017 mmol) in CHCl3 (1.6 mL) using I2 (0.3 mg, 1.2 × 10−3 mmol, 7 mol %), in a reaction time of 1.5 h, to yield isomer (2Z,4E)-6c as a yellow solid (4.0 mg, 89%). Rf (SiO2, 30% EtOAc in hexanes): 0.47. 1H-NMR (CDCl3): δ 8.21 (d, Ar-H, 2H, J = 8.8 Hz), 7.60 (d, Ar-H,2H, J = 8.8 Hz), 7.23 (dd, 1H, J = 15.6; 11.2 Hz), 6.83 (d, 1H, J = 15.6 Hz), 6.65 (dd, 1H, J = 31.7; 11.2 Hz), 3.79 (s, 3H, OCH3), 3.28 (s, 3H, CH3). 13C-NMR (CDCl3): δ 162.3 (d, C= O, 2JCF = 26.6 Hz), 151.8 (d, C-F, 1JCF = 280.1 Hz), 147.6, 142.9, 134.7 (d, 4JCF = 4.6 Hz), 127.6, 124.4, 123.6 (d, 3JCF = 3.7 Hz), 116.8 (d, 2JCF = 9.2 Hz), 62.2 (d, 5JCF = 2.3 Hz), 34.2. 19F-NMR (CDCl3): δ −119.6 (d, 3JHF = 30.5 Hz).
(2Z,4E)-2-Fluoro-N-methoxy-N-methyl-5-(thiophen-2-yl)penta-2,4-dienamide (2Z,4E)-6d. Isomerization was performed with (2Z,4E/Z)-6d (12.0 mg, 0.050 mmol) in CHCl3 (7.5 mL) using I2 (1.2 mg, 4.7 × 10−3 mmol, 10 mol %), in an overnight reaction, to yield isomer (2Z,4E)-6d as an off-white solid (11.0 mg, 92%). Rf (SiO2, 30% EtOAc in hexanes): 0.34. 1H-NMR (CDCl3): δ 7.26 (d, 1H, Ar-H, J = 5.4 Hz), 7.09 (d, 1H, Ar-H, J = 3.4 Hz), 7.00 (dd, 1H, Ar-H, J = 5.1; 3.7 Hz), 6.92 (d, 1H, J = 15.6 Hz), 6.86 (dd, 1H, J = 15.6; 10.7 Hz), 6.61 (dd, 1H, J = 32.2; 10.7 Hz), 3.77 (s, 3H, OCH3), 3.26 (s, 3H, CH3). 13C-NMR (CDCl3): δ 162.7 (d, 2JCF = 26.5 Hz), 150.1 (d, 1JCF = 275.5 Hz), 142.1 (d, J = 2.3 Hz), 130.4 (d, 4JCF = 5.0 Hz), 128.1 (d, J = 1.8 Hz), 128.0, 126.5 (d, J = 1.4 Hz), 118.9 (d, 3JCF = 3.2 Hz), 117.9 (d, 2JCF = 9.6 Hz), 62.1 (d, J = 2.7 Hz), 34.3. 19F-NMR (CDCl3): δ −123.7 (d, 3JHF = 30.5 Hz).

4. Conclusions

In conclusion, we have developed a highly modular approach to (2Z,4E)-2-fluoro-2,4-dienamides. This was achieved via two sequential Julia-Kocienski olefinations. In the first olefination, a Z-α-fluorovinyl Weinreb amide unit, with a benzothiazolylsulfanyl substituent at the allylic position, was assembled. For this, two key building blocks, a known fluorinated Julia-Kocienski reagent with a Weinreb amide moiety (1) and 2-(benzo[d]thiazol-2-ylthio)acetaldehyde (2), a precursor to the second Julia-Kocienski reagent, were reacted. Condensation proceeded with high Z-stereoselectivity and in a good 76% yield. Oxidation of the sulfide to the sulfone furnished the “second-generation” Julia-Kocienski olefination reagent, which underwent reactions with aldehydes to furnish the dienamides in 50%–74% yields. The second set of olefinations proceeded under DBU-mediated conditions and with Z-stereoselectivity. Isomeric (2Z,4E/Z)-mixtures underwent iodine-mediated isomerization to a single (2Z,4E)-dienamide isomer. Although the method was performed with a Weinreb amide moiety, it is potentially applicable to other amides as well. Moreover, due to versatile chemistry of the Weinreb amide moiety, the (2Z,4E)-2-fluoro Weinreb dienamides are potentially useful synthetic building blocks, which can undergo a variety of conversions leading to more complex molecules. In this context, the present method offers a straightforward access to synthetically valuable entities that are not otherwise easily prepared by traditional synthetic approaches to Weinreb amides.

Supplementary Materials

Supplementary materials can be accessed at: https://www.mdpi.com/1420-3049/19/4/4418/s1.

Acknowledgments

This work was supported by NSF Grant CHE-1058618 and a PSC CUNY award. Infrastructural support was provided by NIH NCRR Grant 2G12RR03060-26A1 and by NIMHD Grant 8G12MD007603-27.

Conflicts of Interest

The authors declare no conflict of interest.

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MDPI and ACS Style

Chowdhury, M.; Mandal, S.K.; Banerjee, S.; Zajc, B. Synthesis of Regiospecifically Fluorinated Conjugated Dienamides. Molecules 2014, 19, 4418-4432. https://doi.org/10.3390/molecules19044418

AMA Style

Chowdhury M, Mandal SK, Banerjee S, Zajc B. Synthesis of Regiospecifically Fluorinated Conjugated Dienamides. Molecules. 2014; 19(4):4418-4432. https://doi.org/10.3390/molecules19044418

Chicago/Turabian Style

Chowdhury, Mohammad, Samir K. Mandal, Shaibal Banerjee, and Barbara Zajc. 2014. "Synthesis of Regiospecifically Fluorinated Conjugated Dienamides" Molecules 19, no. 4: 4418-4432. https://doi.org/10.3390/molecules19044418

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