2-Methylpropan-2-ammonium [(3R,5R)-7-[(1S,2S,6S,8S,8aR)-6-hydroxy-2-methyl-8-[(2S)-2-methylbutanoyl]oxy-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-heptanoate

Abstract

Pravastatin is a popular statin agent with applications in the treatment of cardiovascular diseases for patients with an abnormal lipid panel. The starting form of pravastatin is amorphous and following recrystallization, it becomes a crystalline solid with tert-butylamine salt molecules embedded within the lattice. Its molecular and crystal structure were elucidated based on single-crystal X-ray diffraction and characterized by ss-NMR.

1. Introduction

Statins represent a family of agents with applications in the treatment of cardiovascular diseases, which work via the cholesterol-lowering pathway [1,2]. Pravastatin [(3R,5R)-7-[(1S,2S,6S,8S,8aR)-6-hydroxy-2-methyl-8-[(2S)-2-methylbutanoyl]oxy-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoic acid] (Figure 1a) is a medication included in this class that is medically used in the treatment of dyslipidemia [3,4].

In the investigation of active pharmaceutical ingredients from a pharmaceutical point of view, certain parameters such as bioavailability, pharmacokinetics, dissolution rate and solubility are frequently studied [5]. Improving one of these aspects can be achieved using various methods including the formation of salts [6], preparation of nano emulsions [7], complexation with cyclodextrins [8,9,10,11], lipid formulations [12] and preparation of cocrystals and polymorphs [13]. Solid forms of pharmaceutical compounds are found in crystalline and amorphous forms and crystalline forms are thermodynamically more stable than amorphous forms. In general, it has been observed that the amorphous forms of pharmaceutics exhibit higher solubility in comparison with crystalline solids [14].

The aim of this study was to achieve the preparation of pravastatin in a crystalline form, which was successfully prepared as a tert-butylamine salt (denoted Prav-tbua, Figure 1b), the elucidation of its crystal structure via X-ray crystallography and its characterization from a structural point of view.

2. Results

2.1. X-ray Structure Analysis of Prav-tbua

The analysis of Prav-tbua by single-crystal X-ray diffraction revealed that the structure belongs to the orthorhombic P2₁2₁2₁ space group (

Table 1. Crystallographic details related to the investigated compound.

Identification Code	Prav-tbua
Empirical formula	C27H47NO7
Formula weight	497.65
Temperature/K	293(2)
Crystal system	orthorhombic
Space group	P212121
a/Å	5.98809(13)
b/Å	17.4955(3)
c/Å	28.0358(6)
α/°	90
β/°	90
γ/°	90
Volume/Å3	2937.17(10)
Z	4
ρcalc g/cm3	1.125
μ/mm−1	0.648
F(000)	1088.0
Radiation	CuKα (λ = 1.54184)
2Θ range/°	6.306 to 143.05
Index ranges	−7 ≤ h ≤ 7, −19 ≤ k ≤ 21, −25 ≤ l ≤ 33
Reflections collected	12,408
Independent reflections	5198 [Rint = 0.0350, Rsigma = 0.0643]
Data/restraints/parameters	5198/1/329
Goodness-of-fit on F2	1.061
Final R indexes [I ≥ 2σ (I)]	R1 = 0.0646, wR2 = 0.1716
Final R indexes [all data]	R1 = 0.1060, wR2 = 0.1890
Largest diff. peak/hole/e Å−3	0.29/−0.18
Flack parameter	0.12(11)

). The asymmetric unit is depicted in Figure 2a and the compound crystallizes in a stoichiometric ratio of 1:1 pravastatin to solvent molecules. It should be noted that the carboxyl group of pravastatin is deprotonated and the amino group of the solvent molecule gains the hydrogen. The crystal packing and formation of supramolecular self-arrangements are driven by trifurcated N-H···O hydrogen bonds (1.864 Å, 1.874 Å and 1.941 Å) between the protonated amino of solvent molecules with the deprotonated carboxyl group, which are arranged in layers (Figure 2b) and adopt a R³₄ (10) graph set motif. O5-H5···O4 interactions (2.068 Å) also take place between hydroxyl groups that connect the neighboring layers. The overall packing perspective along the a-axis is illustrated in Figure 2c.

Recent studies have focused on the crystal structure of tert-octylamine salt of pravastatin, which monoclinically crystallizes in the P2₁ space group where the migration of protons from carboxylic acid is similar to the migration in the title crystal [15].

2.2. Solid-State NMR Analysis

The ¹H MAS NMR spectrum (Figure 3) showed strongly overlapped lines in the downfield region (0–9 ppm) and one deshielded signal for the protons involved in strong hydrogen bonds. This hydrogen is gained by the amino group of the tert-butylamine molecule as indicated by the single-crystal X-ray structural model and confirmed by the fact that C1–O1 and C1–O2 bond lengths have similar values, i.e., 1.246 and 1.260 Å. Geometrical features of neutral carboxylic groups (C–O bonds are longer than C=O) are different from those of a carboxylate anion, where depending on the extent of delocalization of negative charge between the oxygen atoms, there can be practically no difference between the C–O and C=O distances [16].

The ¹³C spectrum shown in Figure 4 presents very narrow spectral lines specific to a highly crystalline solid.

3. Materials and Methods

3.1. General and Sample Preparations

Pravastatin found as amorphous white powder was purchased from AHH Chemical Co., Ltd., Changzhou, China. The solvents (tert-butylamine, ethanol and hexane) were received from Sigma Aldrich and were used without further purification.

Suitable single crystals of Prav-tbua for X-ray analysis were successfully grown as transparent crystals using vapor diffusion of solids. First, 50 mg (0.12 mmol) of pravastatin was weighed in a 4 mL vial, which was placed in a 20 mL beaker containing 5 mL of ethanol and tert-butylamine mixture in a 1:1 ratio. The beaker was covered with parafilm and held at room temperature for 7 days. The crystals obtained were filtrated and washed with 2 × 1 mL hexane.

3.2. X-ray Diffraction and Structure Refinement

The diffraction data were collected at room temperature using a SuperNova diffractometer equipped with dual X-ray sources (Mo and Cu) (Rigaku, Tokyo, Japan), an Eos CCD detector and an operating tube at 50 kV and 0.08 mA. The crystallographic data were collected and corrected for Lorentz, adsorption and polarization effects using the CrysAlis PRO program [17]. Using Olex2 software, version 1.2.10 [18], the crystal structure was solved with the Superflip solution program [19] using Charge Flipping and refined with ShelXL [20] via least squares minimization.

Crystal Data: Empirical formula: C₂₇H₄₇NO₇ (M = 497.65 g/mol): orthorhombic, space group P2₁2₁2₁ (no. 19), a = 5.98809(13) Å, b = 17.4955(3) Å, c = 28.0358(6) Å, V = 2937.17(10) ų, Z = 4, T = 293(2) K, μ(CuKα) = 0.648 mm⁻¹, Dcalc = 1.125 g/cm³, 12,408 reflections measured (6.306° ≤ 2Θ ≤ 143.05°); 5198 unique (R_int = 0.0350, R_sigma = 0.0643), which were used in all calculations. The final R₁ was 0.0646 (I > 2σ(I)) and wR₂ was 0.1890 (all data). The data are available as Supplementary Materials (CIF file).

3.3. ¹³C Solid-State NMR

The ¹H and ¹³C solid-state NMR spectra were acquired with a Bruker Avance III 500 wide-bore spectrometer (Bruker Biospin, Ettlingen, Germany) operating at 499.98 MHz Larmor frequency for ¹H and 125.73 MHz for ¹³C at room temperature. For the ¹H spectrum, a 1.3 mm double resonance MAS probe head was used with a sample spinning frequency of 60 kHz and no homonuclear decoupling. This spectrum was referenced to a single resonance observed in adamantane for protons at 1.8 ppm with respect to neat tetramethylsilane (TMS). For the ¹³C spectrum, a 4 mm double resonance (1H/X) MAS probe was used with 14 kHz frequency, and a standard ¹³C CP-MAS pulse sequence with a contact pulse time of 2 ms. The spectrum was recorded under high-power proton decoupling (100 kHz) with a TPPM (Two-Pulse Phase Modulation) sequence by averaging 100 transients, with a recycle delay of 5 s. The recorded ¹³C NMR spectrum is calibrated with respect to the CH₃ line in TMS (tetramethylsilane) through an indirect procedure that uses α-Glycine (176.5 ppm for the ¹³COOH line) as an external reference.

4. Conclusions

Starting from amorphous pravastatin, we successfully prepared a crystalline form of pravastatin tert-butylamine salt whose crystal structure was determined by single-crystal X-ray diffraction and further analyzed by ss-NMR.