US20010051738A1

US20010051738A1 - Crystalline1alpha,24(S)-dihydroxyvitamin D2 and method of purification thereof

Info

Publication number: US20010051738A1
Application number: US09/887,297
Authority: US
Inventors: Hector DeLuca; Rafal Sicinski; Hazel Holden; James Thoden
Original assignee: Wisconsin Alumni Research Foundation
Current assignee: Wisconsin Alumni Research Foundation
Priority date: 1999-07-01
Filing date: 2001-06-22
Publication date: 2001-12-13
Also published as: WO2001002352A9; AU5292200A; WO2001002352A1; US6362350B1

Abstract

A method of purifying 1α,24(S)-dihydroxyvitamin D₂to obtain 1α,24(S)-dihydroxyvitamin D₂in crystalline form. The method includes the steps of boiling a solvent under inert atmosphere, dissolving a product containing 1α,24(S)-dihydroxyvitamin D₂to be purified in the solvent, cooling the solvent and dissolved product below ambient temperature for a sufficient amount of time to form a precipitate of 1α,24(S)-dihydroxyvitamin D₂crystals, and recovering the 1α,24(S)-dihydroxyvitamin D₂crystals. The purification technique involves using one of several binary solvent systems, namely, acetone and hexane, 2-propanol and hexane, or ethyl formate and petroleum ether.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional Application No. 60/141,967, filed Jul. 1, 1999.[0001]

BACKGROUND AND SUMMARY OF THE INVENTION

The present invention relates to purification of organic compounds, and more particularly to the purification of a pharmacologically important 1α,24(S)-dihydroxyvitamin D2 compound (1α, 24(S)-(OH) ₂D₂) by preparing it in crystalline form.

Purification of organic compounds, especially those designated for pharmaceutical use, is of considerable importance for chemists synthesizing such compounds. Preparation of the compound usually requires many synthetic steps and, therefore, the final product can be contaminated not only with side-products derived from the last synthetic step of the procedure but also with compounds that were formed in previous steps. Even chromatographic purification, which is a very efficient but relatively time-consuming process, does not usually provide compounds which are sufficiently pure to be used as drugs.

Depending on the method used to synthesize 1α-hydroxyvitamin D compounds, different minor undesirable compounds can accompany the final product. Thus, for example, if direct C-1 hydroxylation of 5,6-trans geometric isomer of vitamin D is performed, followed by SeO ₂/NMO oxidation and photochemical irradiation [see Andrews et al., J. Org. Chem. 51, 1635 (1986); Calverley et al., Tetrahedron 43, 4609 (1987); Choudry et al., J. Org. Chem. 58, 1496 (1993)], the final 1α-hydroxyvitamin D product can be contaminated with 1β-hydroxy- as well as 5,6-trans isomers. If the method consists of C-1 allylic oxidation of the 4-phenyl-1,2,4-triazoline-3,5-dione adduct of the previtamin D compound, followed by cycloreversion of the modified adduct under basic conditions [Nevinckx et al., Tetrahedron 47, 9419 (1991); Vanmaele et al., Tetrahedron 41, 141 (1985) and 40, 1179 (1991); Vanmaele et al., Tetrahedron Lett. 23, 995 (1982)], one can expect that the desired 1α-hydroxyvitamin can be contaminated with the previtamin 5(10),6,8-triene and 1β-hydroxy isomer. One of the most useful C-1 hydroxylation methods, of very broad scope and numerous applications, is the experimentally simple procedure elaborated by Paaren et al. [see J. Org. Chem. 45, 3253 (1980) and Proc. Natl. Acad. Sci. U.S.A. 75, 2080 (1978)]. This method consists of allylic oxidation of 3,5-cyclovitamin D derivatives, readily obtained from the buffered solvolysis of vitamin D tosylates, with SeO₂/t-BuOOH and subsequent acid-catalyzed cycloreversion to the desired 1α-hydroxy compounds. Taking into account this synthetic path it is reasonable to assume that the final product can be contaminated with 1β-hydroxy epimer, 5,6-trans isomer and the previtamin D form.

The vitamin D conjugated triene system is not only heat- and light-sensitive but it is also prone to oxidation, leading to the complex mixture of very polar compounds. Oxidation usually happens when a vitamin D compound has been stored for a prolonged time. Other types of processes that can lead to a partial decomposition of vitamin D compounds consist of the some water-elimination reactions; their driving force is the allylic (1α-) and homoallylic (3β-) position of the hydroxy groups. The presence of such above-mentioned oxidation and elimination products can be easily detected by thin-layer chromatography. Thus, for example, using precoated aluminum silica sheets [with UV indicator; from EM Science (Cherry Hill, N.J.)] and solvent system hexane-ethyl acetate (3:7), the spot of 1α,24(S)-(OH) ₂D₂(R_f0.40) and its elimination products (R_f's ca. 0.8-0.9) are visible in ultraviolet light. Also, after spraying with sulfuric acid and heating, an additional spot can be visualized (R_f0), derived from oxidation products.

Usually, all 1α-hydroxylation procedures require at least one chromatographic purification. However, even chromatographically purified 1α,24(S)-dihydroxyvitamin D ₂although showing consistent spectroscopic data, suggesting its homogeneity, does not meet the purity criteria required for therapeutic agents that can be orally, parenterally or transdermally administered. Therefore, it was evident that a suitable method of purification of 1α,24(S)-dihydroxyvitamin D₂is required.

Since it is well known that the simplest procedure that can be used for compound purification is a crystallization process, it has been decided to investigate purification of 1α,24(S)—(OH) ₂D₂by means of crystallization. The solvent plays a crucial role in the crystallization process, and is typically an individual liquid substance or a suitable mixture of different liquids. For crystallizing 1α,24(S)-dihydroxyvitamin D₂, the most appropriate solvent and/or solvent system is characterized by the following factors:

(1) low toxicity;

(2) low boiling point;

(3) significant dependence of solubility properties with regard to temperature (condition necessary for providing satisfactory crystallization yield); and

(4) relatively low cost.

It is believed that highly apolar solvents (e.g. hydrocarbons) were not suitable due to their low solubility potency. Quite the reverse situation occurred in the highly polar media (e.g. alcohols), in which 1α, 24(S)—(OH) ₂D₂, showed too high solubility. Therefore, it is concluded that for the successful crystallization of 1α,24(S)—(OH)₂D₂, a solvent mixture is required, consisting of two (or more) solvents differing considerably in polarity. After numerous experiments, it was found that several binary solvent systems were useful for the crystallization of 1α,24(S)—(OH)₂D₂, namely: acetone-hexane, 2-propanol-hexane and ethyl formate-petroleum ether. These solvents are all characterized by low toxicity, and they are very easy to remove by evaporation or other well known methods. In all cases it is believed the crystallization process will occur easily and efficiently, and the precipitated crystals will be sufficiently large to assure their recovery by filtration.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1[0013] a-1 h are graphs of ¹H NMR spectrum (CDCl₃, 500 MHz) of the solid 1α,24(S)-dihydroxyvitamin D₂material before crystallization (FIGS. 1a and 1 b) as well as the spectra of the crystals of 1α,24(S)—(OH)₂D₂which resulted after two crystallizations using the following solvent systems: acetone-hexane (FIGS. 1c and 1 d), 2-propanol-hexane (FIGS. 1e and 1 f) and HCOOEt-petroleum ether (FIGS. 1g and 1 h);
FIGS. 2[0014] a-2 d are HPLC (10 mm×25 cm Zorbax-Sil column, 20% 2-propanol in hexane, 4 mL/min; UV detection at 260 nm) profiles of the solid 1α,24(S)-dihydroxyvitamin D₂material before crystallization (FIG. 2a) and the crystals resulted after two crystallizations using the following solvent systems: acetone-hexane (FIG. 2b), 2-propanol-hexane (FIG. 2c) and HCOOEt-petroleum ether (FIG. 2d). In the region indicated by asterisk (ca. 34 mL) sensitivity was decreased 20 times.
FIGS. 3[0015] a-3 i are HPLC (10 mm×25 cm Zorbax-Sil column, 20% 2-propanol in hexane, 4 mL/min; UV detection at 260 nm) profiles of the crystals of 1α,24(S)-dihydroxyvitamin D₂resulted after single crystallization using the following solvent systems: acetone-hexane (FIG. 3a), 2-propanol-hexane (FIG. 3d) and HCOOEt-petroleum ether (FIG. 3g); the HPLC profiles of mother liquors after single crystallization using the following solvent systems: acetone-hexane (FIG. 3b); 2-propanol-hexane (FIG. 3e) and HCOOEt-petroleum ether (FIG. 3h); and the HPLC profiles of mother liquors after two crystallizations using the following solvent systems: acetone-hexane (FIG. 3c); 2-propanol-hexane (FIG. 3f and HCOOEt-petroleum ether (FIG. 3i). Region with decreased sensitivity (ca. 34 mL) is indicated by asterisk.
FIGS. 4[0016] a-4 d are HPLC (4.6 mm×25 cm Zorbax-Eclipse XDB-C18 column, 20% water in methanol, 1 mL/min; UV detection at 260 nm) profiles of the solid 1α,24(S)-dihydroxyvitamin D₂material before crystallization (FIG. 4a) and the crystals resulted after two crystallizations using the following solvent systems: acetone-hexane (FIG. 4b), 2-propanol-hexane (FIG. 4c) and HCOOEt-petroleum ether (FIG. 4d). In the region indicated by asterisk (ca. 22 mL) sensitivity was decreased 20 times.
FIGS. 5[0017] a-5 c are microscope-magnified images of the crystals of 1α,24(S)-dihydroxyvitamin D₂resulted after two crystallizations from: acetone-hexane (FIG. 5a), 2-propanol-hexane (FIG. 5b) and HCOOEt-petroleum ether (FIG. 5c).
FIG. 6 is an illustration of the three dimensional structure of 1α,24(S)-dihydroxyvitamin D[0018] ₂as defined by the atomic positional parameters discovered and set forth herein.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides a valuable method of purification of 1α,24(S)-dihydroxyvitamin D[0019] ₂, a pharmacologically important compound, characterized by the formula shown below:
The purification technique involves obtaining the 1α,24(S)-dihydroxyvitamin D[0020] ₂product in crystalline form by utilizing a crystallization procedure wherein the 1α,24(S)-dihydroxyvitamin D₂material to be purified is dissolved using as the solvent system one of the following:
(1) acetone and hexane; [0021]
(2) 2-propanol and hexane; or [0022]
(3) ethyl formate and petroleum ether. [0023]
Thereafter, the solvent or solvent system can be removed by evaporation, with or without vacuum, or via other means as is well known. The technique can be used to purify a wide range of final products containing 1α,24(S)-dihydroxyvitamin D[0024] ₂obtained from any known synthesis thereof, and in varying concentrations, i.e. from microgram amounts to kilogram amounts. As is well known to those skilled in this art, the amount of solvent utilized should be minimized and/or adjusted according to the amount of 1α,24(S)-dihydroxyvitamin D₂to be purified.
The usefulness and advantages of the present crystallization procedures is shown in the following specific Examples. Solid 1α,24(S)-dihydroxyvitamin D[0025] ₂product which was purified by chromatography on silica and was used as a suitable starting material. This material showed reasonably good 500 MHz ¹H NMR spectrum (FIGS. 1a, 1 b), but concomitant compounds were detected by straight- and reverse-phase HPLC (FIGS. 2a and 4 a, respectively) and, moreover, the presence of some oxidation products was confirmed by TLC (presence of the spot of R_f0). After recrystallization from the solvents listed above, the precipitated material was observed under microscope to confirm its crystalline form (FIGS. 5a-5 c). Additionally, in the case of crystals precipitated from 2-propanol-hexane, X-ray diffraction analysis was performed (FIG. 6). The corresponding crops of crystals were then carefully analyzed and their significantly improved purity was confirmed by straight-phase HPLC (FIGS. 2b, 2 c, 2 d), reverse-phase HPLC (FIGS. 4b, 4 c, 4 d), TLC and 500 MHz ¹H NMR (FIGS. 1c-1 h). Yields of crystallizations were high and the obtained crystals showed a relatively sharp melting point.
The corresponding straight- and reverse-phase HPLC profiles of the recrystallized 1α,24(S)-dihydroxyvitamin D[0026] ₂, shown in FIGS. 2b-2 d and 4 b-4 d, respectively, clearly indicate a considerable improvement in the compound purity. The important observation consists of the significantly diminished proportion of the concomitant 1α,24(R)-dihydroxyvitamin D₂(peak of retention time ca. 30 mL on FIGS. 2b-2 d and ca. 25 mL on FIGS. 4b-4 d) in the recrystallized compound; content of this R-isomer impurity has decreased more than 3 times (3.3-5.3) in respect to its value in the starting 1α,24(S)-dihydroxyvitamin D₂product and does not exceed 0.5%.
The described crystallization process of the synthetic 1α,24(S)-dihydroxyvitamin D[0027] ₂product represents a valuable purification method, which can remove products derived from the synthetic path, including its concomitant 24-epimeric compound, namely, 1α,24(R)-dihydroxyvitamin D₂. Such impurity is a result of the nonstereospecific construction of the side chain (U.S. Pat. Nos. 5,786,348 and 5,789,397). In such case the separation of both epimeric vitamins is necessary and it is usually performed during the last stage of the synthesis. However, column chromatography and straight-phase separation of the 24-epimers is practically impossible due to their similar chromatographical properties, and larger-scale separation is also difficult by reverse-phase HPLC.

CRYSTALLIZATION OF 1α,24-DIHYDROXYVITAMIN D₂

EXAMPLE 1

Crystallization from Acetone-Hexane [0028]
(a) 1α,24(S)-dihydroxyvitamin D[0029] ₂product (25 mg, m.p. 136-142.5° C.) was dissolved in boiling acetone (0.18 mL, Fisher Scientific) under argon atmosphere and hexane (0.72 mL, Burdick & Jackson) was added. The solution was left at room temperature (68° F.) for a few hours and then in a refrigerator (35-45° F.) overnight. The precipitated crystals were filtered off, washed with a small volume of a cold hexane and dried. The yield of crystalline material was 15 mg (60%). HPLC profiles of crystals and mother liquor are shown in FIGS. 3a, 3 b.
(b) These crystals of 1α,24(S)-dihydroxyvitamin D[0030] ₂(12 mg) were recrystallized from acetone (0.07 mL) and hexane (0.3 mL) as described in Example 1(a) and the precipitated crystals (9 mg, 75%), m.p. 146.5-151° C. were observed under a microscope (FIG. 5a) and analyzed by straight-phase HPLC (crystals: FIG. 2b; mother liquors: FIG. 3c), reverse-phase HPLC (FIG. 4b) and ¹H NMR (FIGS. 1c, 1 d).

EXAMPLE 2

Crystallization from 2-Propanol-Hexane [0031]
(a) 1α,24(S)-dihydroxyvitamin D[0032] ₂product (25 mg) was dissolved in a boiling 2-propanol-hexane mixture (1:4, 0.75 mL; Burdick & Jackson) under argon atmosphere, left at room temperature (68° F.) for a few hours and then in a refrigerator (35-45° F.) overnight. The precipitated crystals were filtered off, washed with a small volume of a cold hexane and dried. The yield of crystalline material was 17 mg (68%) HPLC profiles of crystals and mother liquor are shown in FIGS. 3d, 3 e. (b) These crystals of 1α,24(S)-dihydroxyvitamin D₂product (15 mg) were recrystallized from 2-propanol-hexane mixture (1:4, 0.43 mL) as described in Example 2(a) and the precipitated crystals (8 mg, 53%) m.p. 147-151.5° C., were observed under a microscope (FIG. 5b) and analyzed by straight-phase HPLC (crystals: FIG. 2c; mother liquors: FIG. 3f), reverse-phase HPLC (FIG. 4c) and ¹H NMR (FIGS. 1e, 1 f).

EXAMPLE 3

Crystallization from Ethyl Formate-Petroleum Ether [0033]
(a) 1α,24(S)-dihydroxyvitamin D[0034] ₂product (25 mg) was dissolved in boiling ethyl formate (0.5 mL, Aldrich) under argon atmosphere and petroleum ether (1 mL, b.p. 35-60° C.; Aldrich) was added. The solution was left at room temperature (68° F.) for a few hours and then in a refrigerator (35-45° F.) overnight. The precipitated crystals were filtered off, washed with a small volume of a cold hexane and dried. The yield of crystalline material was 17 mg (68%). HPLC profiles of crystals and mother liquor are shown in FIGS. 3g, 3 h.
(b) These crystals of 1α,24(S)-dihydroxyvitamin D[0035] ₂(15 mg) were recrystallized from ethyl formate (0.25 mL) and petroleum ether (0.5 mL) as described in Example 3(a) and the precipitated crystals (9 mg, 60%), m.p. 142-146.5° C., were observed under a microscope (FIG. 5c) and analyzed by straight-phase HPLC (crystals: FIG. 2d; mother liquors, FIG. 3i), reverse-phase HPLC (FIG. 4d) and ¹H NMR (FIGS. 1g, 1 h.).
Experimental [0036]
A colorless prism-shaped crystal of dimensions 0.42×0.17×0.08 mm was selected for structural analysis. Intensity data for this compound were collected using a Bruker SMART ccd area detector, (a) Data collection: SMART Software Reference Manual (1994). Bruker-AXS, 6300 Enterprise Dr., Madison, Wis. 53719-1173, U.S.A., (b) Data Reduction: SAINT Software Reference Manual (1995). Brunker-AXS, 6300 Enterprise Drive, Madison, Wis. 53719-1173, U.S.A., mounted on a Bruker Platform goniometer using graphite-monochromated Mo Kα radiation (λ=0.71073 Å). The sample was cooled to 133K. The intensity data, which nominally covered one and a half hemispheres of reciprocal space, were measured as a series of ω oscillation frames each of 0.3° for 90 sec/frame. The detector was operated in 512×512 mode and was positioned 5.00 cm from the sample. Coverage of unique data was 99.9 % complete to 25.00 degrees in θ. Cell parameters were determined from a non-linear least squares fit of 5435 peaks in the range 2.30<θ<28.28°. The first 50 frames were repeated at the end of data collection and yielded 156 peaks showing a variation of 0.01% during the data collection. A total of 9896 data were measured in the range 1.61<θ<28.30°. The data were corrected for absorption by the empirical method G. M. Sheldrick (1996). SADABS. Program for Empirical Absorption Correction of Area Detector Data. University of Göttingen, Germany, giving minimum and maximum transmission factors of 0.769 and 0.970. The data were merged to form a set of 7019 independent data with R(int)=0.0389. [0037]
The monoclinic space group P2(1) was determined by systematic absences and statistical tests and verified by subsequent refinement. The structure was solved by direct methods and refined by full-matrix least-squares methods on F[0038] ^{2, (a)}G. M. Sheldrick (1994). SHELXTL Version 5 Reference Manual, Bruker-AXS, 6300 Enterprise Drive, Madison, Wis. 53719-1173, U.S.A. (b) International Tables for Crystallography, Vol. C, Tables 6.1.1.4, 4.2.6.8, and 4.2.4.2, Kluwer: Boston (1995). Hydrogen atom positions were initially determined by geometry and refined by a riding model. Non-hydrogen atoms were refined with anisotropic displacement parameters. A total of 353 parameters were refined against 7 restraints and 7019 data to give wR(F²)=0.1274 and S=0.952 for weights of w=1/[σ²(F²)+(0.0670 p)²], where P=[F_o ²+2F_c ²]/3. The final R(F) was 0.0504 for the 5187 observed, [F>4σ(F)], data. The largest shift/s.u. was 0.006 in the final refinement cycle. The final difference map had maxima and minima of 0.241 and −0.155 e/Å³, respectively. The absolute structure was determined by refinement of the Flack parameter, H. D. Flack, Acta Cryst. A39, 876-881 (1983). The polar axis restraints were taken from Flack and Schwarzenbach, H. D. Flack and D. Schwarzenback, Acta Cryst. A44, 499-506 (1988).
The displacement ellipsoids are drawn at the 50% probability level in FIG. 6. The solvent molecule of 2-propanol was disordered and modeled in two orientations with occupancies of 0.473(10) and 0.527(10) for the unprimed and primed atoms (not shown in FIG. 6). Restraints on the positional parameters of the solvent were required for the refinement to achieve convergence. [0039]

The three dimensional structure of 1α,24(S)-dihydroxyvitamnin D ₂as defined by the following physical data and atomic positional parameters described and calculated herein is illustrated in FIG. 6.

TABLE 1


Crystal data and structure refinement for 1α,24(S)-dihydroxyvitamin D₂.

Empirical formula	(C28 H44 O3) (C3 H8 O)
Formula weight	488.73
Crystal system	Monoclinic
Space group	P2(1)

Unit cell dimensions	a = 12.8196(11) Å	α = 90°
	b = 7.6363(6) Å	β = 99.270(2)°
	c = 15.4915(13) Å	γ = 90°

Volume	1496.7(2) Å³
Z	2
Density (calculated)	1.084 Mg/m³
Wavelength	0.71073 Å
Temperature	133(2) K
F(000)	540
Absorption coefficient	0.069 mm⁻¹
Absorption correction	Empirical
Max. and min. transmission	0.970 and 0.769
Theta range for data collection	1.61 to 28.30°.
Reflections collected	9896
Independent reflections	7019 [R(int) = 0.0389]
Data/restraints/parameters	7019/7(disorder)/353
wR(F²all data)	wR2 = 0.1274
R(F obsd data)	R1 = 0.0504
Goodness-of-fit on F²	0.952
Observed data [I > 2σ(I)]	5187
Absolute structure parameter	−1.3(11)
Largest and mean shift/s.u.	0.006 and 0.000
Largest diff. peak and hole	0.241 and −0.155 e/Å³

TABLE 2


Atomic coordinates and equivalent isotropic displacement parameters
for 1α,24(S)-dihydroxyvitamin D₂. U(eq) is defined as one third of the
trace of the orthogonalized U_ijtensor.

	x	y	z	U(eq)

O(1)	0.74103(14)	0.26699(19)	0.64786(9)	0.0504(4)
O(2)	0.71159(11)	0.81818(19)	0.65629(8)	0.0398(3)
O(3)	0.71370(12)	0.0537(2)	−0.21338(9)	0.0422(4)
C(1)	0.75494(16)	0.4442(3)	0.62449(12)	0.0340(4)
C(2)	0.78823(16)	0.5444(3)	0.70961(11)	0.0358(4)
C(3)	0.80863(15)	0.7362(3)	0.69351(12)	0.0347(4)
C(4)	0.88914(16)	0.7581(3)	0.63196(12)	0.0377(5)
C(5)	0.85897(14)	0.6546(3)	0.54858(12)	0.0332(4)
C(6)	0.85205(15)	0.7322(3)	0.47018(12)	0.0363(4)
C(7)	0.82031(15)	0.6503(3)	0.38543(12)	0.0351(4)
C(8)	0.81345(15)	0.7288(3)	0.30735(12)	0.0355(4)
C(9)	0.83815(19)	0.9172(3)	0.29164(13)	0.0438(5)
C(10)	0.83535(15)	0.4674(3)	0.56360(12)	0.0332(4)
C(11)	0.90937(19)	0.9379(3)	0.22164(13)	0.0439(5)
C(12)	0.86813(17)	0.8370(3)	0.13713(12)	0.0381(5)
C(13)	0.85111(14)	0.6444(3)	0.15568(11)	0.0302(4)
C(14)	0.77427(15)	0.6343(3)	0.22337(12)	0.0332(4)
C(15)	0.74419(18)	0.4419(3)	0.22396(13)	0.0426(5)
C(16)	0.73673(17)	0.3872(3)	0.12732(12)	0.0386(5)
C(17)	0.78577(14)	0.5385(3)	0.07984(11)	0.0310(4)
C(18)	0.95630(15)	0.5526(3)	0.18950(13)	0.0408(5)
C(19)	0.88104(18)	0.3357(3)	0.52951(15)	0.0485(6)
C(20)	0.83816(16)	0.4686(3)	0.00427(12)	0.0344(4)
C(21)	0.89386(18)	0.6079(3)	−0.04330(13)	0.0431(5)
C(22)	0.75293(16)	0.3790(3)	−0.05931(12)	0.0345(4)
C(23)	0.74996(16)	0.2140(3)	−0.08077(12)	0.0352(4)
C(24)	0.66492(16)	0.1167(3)	−0.14141(12)	0.0331(4)
C(28)	0.57047(17)	0.2288(3)	−0.17729(14)	0.0428(5)
C(25)	0.63467(17)	−0.0501(3)	−0.09445(13)	0.0389(5)
C(26)	0.5682(2)	−0.1799(3)	−0.15392(16)	0.0490(6)
C(27)	0.5808(2)	−0.0051(3)	−0.01633(15)	0.0537(6)
O(1S)	0.6790(4)	0.0433(9)	0.5132(5)	0.0525(15)
C(1S)	0.5785(5)	0.0407(9)	0.4589(4)	0.0579(19)
C(2S)	0.568(2)	0.193(2)	0.3972(15)	0.082(6)
C(3S)	0.5668(13)	−0.1295(19)	0.4094(16)	0.068(4)
O(1S′)	0.6310(6)	0.0515(8)	0.5266(3)	0.0531(15)
C(1S′)	0.6298(6)	0.0414(9)	0.4348(3)	0.0622(19)
C(2S′)	0.589(2)	0.216(2)	0.4011(14)	0.091(5)
C(3S′)	0.5714(16)	−0.117(2)	0.3957(17)	0.104(8)

TABLE 3


Bond lengths [Å] and angles [°] for 1α,24(S)-dihydroxyvitamin D₂.

O(1)—C(1)	1.419(2)	C(13)—C(17)	1.556(2)
O(2)—C(3)	1.429(2)	C(14)—C(15)	1.519(3)
O(3)—C(24)	1.446(2)	C(15)—C(16)	1.542(3)
C(1)—C(10)	1.516(3)	C(16)—C(17)	1.556(3)
C(1)—C(2)	1.525(3)	C(17)—C(20)	1.536(3)
C(2)—C(3)	1.515(3)	C(20)—C(22)	1.512(3)
C(3)—C(4)	1.523(3)	C(20)—C(21)	1.534(3)
C(4)—C(5)	1.511(3)	C(22)—C(23)	1.303(3)
C(5)—C(6)	1.341(3)	C(23)—C(24)	1.514(3)
C(5)—C(10)	1.487(3)	C(24)—C(28)	1.514(3)
C(6)—C(7)	1.452(3)	C(24)—C(25)	1.547(3)
C(7)—C(8)	1.340(3)	C(25)—C(26)	1.518(3)
C(8)—C(9)	1.501(3)	C(25)—C(27)	1.526(3)
C(8)—C(14)	1.502(3)	O(1S)—C(1S)	1.421(5)
C(9)—C(11)	1.534(3)	C(1S)—C(2S)	1.500(6)
C(10)—C(19)	1.317(3)	C(1S)—C(3S)	1.504(6)
C(11)—C(12)	1.537(3)	O(1S′)—C(1S′)	1.422(5)
C(12)—C(13)	1.521(3)	C(1S′)—C(2S′)	1.498(6)
C(13)—C(18)	1.535(3)	C(1S′)—C(3S′)	1.501(6)
C(13)—C(14)	1.552(3)
O(1)—C(1)—C(10)	113.37(16)	C(8)—C(9)—C(11)	112.23(18)
O(1)—C(1)—C(2)	106.70(15)	C(19)—C(10)—C(5)	123.8(2)
C(10)—C(1)—C(2)	110.83(16)	C(19)—C(10)—C(1)	123.4(2)
C(3)—C(2)—C(1)	112.00(15)	C(5)—C(10)—C(1)	112.72(16)
O(2)—C(3)—C(2)	109.14(16)	C(9)—C(11)—C(12)	112.84(17)
O(2)—C(3)—C(4)	109.44(16)	C(13)—C(12)—C(11)	111.33(16)
C(2)—C(3)—C(4)	111.21(17)	C(12)—C(13)—C(18)	111.18(17)
C(5)—C(4)—C(3)	111.82(16)	C(12)—C(13)—C(14)	107.58(16)
C(6)—C(5)—C(10)	125.50(18)	C(18)—C(13)—C(14)	111.39(15)
C(6)—C(5)—C(4)	120.90(19)	C(12)—C(13)—C(17)	115.88(15)
C(10)—C(5)—C(4)	113.57(17)	C(18)—C(13)—C(17)	110.89(16)
C(5)—C(6)—C(7)	126.6(2)	C(14)—C(13)—C(17)	99.28(14)
C(8)—C(7)—C(6)	126.2(2)	C(8)—C(14)—C(15)	120.64(17)
C(7)—C(8)—C(9)	126.19(18)	C(8)—C(14)—C(13)	113.65(15)
C(7)—C(8)—C(14)	122.04(19)	C(15)—C(14)—C(13)	103.99(16)
C(9)—C(8)—C(14)	111.73(17)	C(14)—C(15)—C(16)	103.42(17)
C(15)—C(16)—C(17)	106.93(16)	O(3)—C(24)—C(25)	105.13(15)
C(20)—C(17)—C(13)	120.53(15)	C(28)—C(24)—C(25)	113.08(18)
C(20)—C(17)—C(16)	111.23(17)	C(23)—C(24)—C(25)	108.79(16)
C(13)—C(17)—C(16)	103.81(14)	C(26)—C(25)—C(27)	110.29(18)
C(22)—C(20)—C(21)	110.13(16)	C(26)—C(25)—C(24)	114.26(17)
C(22)—C(20)—C(17)	107.15(15)	C(27)—C(25)—C(24)	111.56(18)
C(21)—C(20)—C(17)	114.81(17)	O(15)—C(15)—C(25)	110.1(12)
C(23)—C(22)—C(20)	126.32(19)	O(15)—C(15)—C(35)	108.7(8)
C(22)—C(23)—C(24)	128.42(19)	C(2S)—C(1S)—C(3S)	110.9(15)
O(3)—C(24)—C(28)	108.95(16)	O(1S′)—C(1S′)—C(2S′)	104.3(9)
O(3)—C(24)—C(23)	106.50(15)	O(1S′)—C(1S′)—C(3S′)	111.8(12)
C(28)—C(24)—C(23)	113.83(17)	C(2S′)—C(1S′)—C(3S′)	117.1(14)

TABLE 4


Anisotropic displacement parameters (Å²× 10³) for 1α,24(S)-
dihydroxyvitamin D₂. The anisotropic displacement factor exponent
takes the form: −2π²[h²α²U₁₁+ ... + 2hkαb* U₁₂]

	U₁₁	U₂₂	U₃₃	U₂₃	U₁₃	U₁₂

O(1)	84(1)	39(1)	30(1)	0(1)	15(1)	−10(1)
O(2)	49(1)	41(1)	29(1)	−8(1)	4(1)	8(1)
O(3)	61(1)	40(1)	31(1)	8(1)	22(1)	−2(1)
C(2)	44(1)	43(1)	22(1)	0(1)	10(1)	3(1)
C(3)	44(1)	40(1)	21(1)	−7(1)	4(1)	1(1)
C(4)	41(1)	46(1)	26(1)	−7(1)	3(1)	−9(1)
C(5)	28(1)	47(1)	25(1)	−7(1)	7(1)	−3(1)
C(6)	37(1)	44(1)	29(1)	−5(1)	8(1)	−10(1)
C(7)	35(1)	47(1)	25(1)	−4(1)	9(1)	10(1)
C(8)	35(1)	47(1)	25(l)	−4(1)	8(1)	−6(1)
C(9)	59(1)	46(1)	28(1)	−8(1)	9(1)	−6(1)
C(10)	33(1)	43(1)	23(1)	−4(1)	2(1)	2(1)
C(11)	60(1)	40(1)	32(1)	−3(1)	10(1)	−14(1)
C(12)	46(1)	43(1)	27(1)	0(1)	9(1)	−8(1)
C(13)	30(1)	40(1)	21(1)	−1(1)	6(1)	−5(1)
C(14)	33(1)	44(1)	24(1)	−2(1)	7(1)	−6(1)
C(15)	49(1)	54(1)	25(1)	−5(1)	8(1)	20(1)
C(16)	44(1)	48(1)	25(1)	−5(1)	7(1)	12(1)
C(17)	32(1)	39(1)	22(1)	−3(1)	4(1)	−2(1)
C(18)	35(1)	54(1)	32(1)	−2(1)	0(1)	0(1)
C(19)	49(1)	57(1)	40(1)	−8(1)	9(1)	6(1)
C(20)	38(1)	41(1)	24(1)	−5(1)	7(1)	1(1)
C(21)	47(1)	54(1)	31(1)	5(1)	15(1)	−5(1)
C(22)	41(1)	41(1)	22(1)	−2(1)	5(1)	5(1)
C(23)	37(1)	43(1)	26(1)	−1(1)	9(1)	3(1)
C(24)	41(1)	35(1)	26(1)	−7(1)	10(1)	1(1)
C(28)	47(1)	45(1)	35(1)	−5(1)	1(1)	3(1)
C(25)	43(1)	43(1)	33(1)	0(1)	11(1)	2(1)
C(26)	60(1)	43(1)	48(1)	−7(1)	20(1)	−9(1)
C(27)	68(2)	63(2)	35(1)	−4(1)	23(1)	−16(1)
O(1S)	71(4)	47(2)	35(3)	0(2)	−4(3)	−6(3)
C(1S)	46(4)	86(4)	44(4)	2(3)	13(3)	3(3)
C(2S)	52(7)	116(10)	76(9)	42(9)	7(6)	29(9)
C(3S)	43(6)	108(10)	51(6)	−34(5)	−1(4)	−2(6)
O(1S′)	78(4)	50(2)	30(2)	5(2)	4(2)	3(3)
C(1S′)	49(4)	102(5)	35(3)	−4(3)	4(2)	3(3)
C(2S′)	73(10)	139(11)	56(6)	33(6)	−3(5)	−10(6)
C(3S′)	81(9)	165(15)	66(9)	−44(8)	10(6)	−40(9)

TABLE 5


Hydrogen coordinates and isotropic displacement parameters for
1α,24(S)-dihydroxyvitamin D₂.

	x	y	z	U(eq)

H(1O)	0.7154	0.2011	0.5980	0.060
H(2O)	0.6925	0.9129	0.6947	0.048
H(3O)	0.7209	0.1479	−0.2497	0.051
H(1)	0.6854	0.4912	0.5950	0.041
H(2A)	0.7320	0.5346	0.7462	0.043
H(2B)	0.8532	0.4910	0.7422	0.043
H(3)	0.8363	0.7938	0.7506	0.042
H(4A)	0.8946	0.8837	0.6174	0.045
H(4B)	0.9593	0.7188	0.6619	0.045
H(6)	0.8697	0.8530	0.4701	0.044
H(7)	0.8027	0.5294	0.3853	0.042
H(9A)	0.8737	0.9699	0.3471	0.053
H(9B)	0.7713	0.9816	0.2730	0.053
H(11A)	0.9812	0.8955	0.2455	0.053
H(11B)	0.9148	1.0637	0.2076	0.053
H(12A)	0.8005	0.8892	0.1088	0.046
H(12B)	0.9196	0.8477	0.0961	0.046
H(14)	0.7088	0.6975	0.1962	0.040
H(15A)	0.6756	0.4260	0.2445	0.051
H(15B)	0.7990	0.3732	0.2619	0.051
H(16A)	0.6620	0.3686	0.1007	0.046
H(16B)	0.7761	0.2770	0.1227	0.046
H(17)	0.7260	0.6153	0.0532	0.037
H(18A)	1.0078	0.5807	0.1512	0.061
H(18B)	0.9452	0.4256	0.1899	0.061
H(18C)	0.9831	0.5928	0.2490	0.061
H(19A)	0.9324	0.3576	0.4929	0.058
H(19B)	0.8627	0.2186	0.5415	0.058
H(20)	0.8916	0.3785	0.0284	0.041
H(21A)	0.9193	0.5545	−0.0935	0.065
H(21B)	0.9539	0.6561	−0.0031	0.065
H(21C)	0.8440	0.7021	−0.0636	0.065
H(22)	0.6960	0.4500	−0.0862	0.041
H(23)	0.8088	0.1457	−0.0550	0.042
H(25A)	0.7023	−0.1109	−0.0706	0.047
H(26A)	0.6064	−0.2152	−0.2010	0.074
H(26B)	0.5011	−0.1250	−0.1791	0.074
H(26C)	0.5543	−0.2832	−0.1200	0.074
H(27A)	0.6233	0.0815	0.0205	0.081
H(27B)	0.5739	−0.1112	0.0179	0.081
H(27C)	0.5105	0.0434	−0.0372	0.081
H(28A)	0.5940	0.3296	−0.2083	0.064
H(28B)	0.5360	0.2701	−0.1290	0.064
H(28C)	0.5202	0.1593	−0.2178	0.064
H(1S)	0.6790	−0.0276	0.5547	0.063
H(1S1)	0.5221	0.0487	0.4964	0.069
H(2S1)	0.5939	0.2994	0.4296	0.123
H(2S2)	0.4940	0.2087	0.3714	0.123
H(2S3)	0.6104	0.1727	0.3507	0.123
H(3S1)	0.6057	−0.1162	0.3603	0.102
H(3S2)	0.4918	−0.1495	0.3870	0.102
H(3S3)	0.5952	−0.2295	0.4454	0.102
H(1S′)	0.6602	−0.0383	0.5507	0.064
H(1S2)	0.7047	0.0316	0.4246	0.075
H(2S4)	0.5199	0.2383	0.4191	0.136
H(2S5)	0.5804	0.2165	0.3371	0.136
H(2S6)	0.6385	0.3081	0.4247	0.136
H(3S4)	0.6045	−0.2183	0.4284	0.156
H(3S5)	0.5751	−0.1324	0.3334	0.156
H(3S6)	0.4973	−0.1090	0.4037	0.156

TABLE 6


Torsion angles [°] for 1α,24(S)-dihydroxyvitamin D₂.

		C(12)—C(13)—C(14)—C(15)	168.80(16)
O(1)—C(1)—C(2)—C(3)	178.48(16)	C(18)—C(13)—C(14)—C(15)	−69.1(2)
C(10)—C(1)—C(2)—C(3)	54.6(2)	C(17)—C(13)—C(14)—C(15)	47.76(18)
C(1)—C(2)—C(3)—O(2)	66.0(2)	C(8)—C(14)—C(15)—C(16)	−166.13(18)
C(1)—C(2)—C(3)—C(4)	−54.8(2)	C(13)—C(14)—C(15)—C(16)	−37.2(2)
O(2)—C(3)—C(4)—C(5)	−68.2(2)	C(14)—C(15)—C(16)—C(17)	11.8(2)
C(2)—C(3)—C(4)—C(5)	52.5(2)	C(12)—C(13)—C(17)—C(20)	80.8(2)
C(3)—C(4)—C(S)—C(6)	126.3(2)	O(18)—C(13)—C(17)—C(20)	−47.1(2)
C(3)—C(4)—C(5)—C(10)	−51.6(2)	O(14)—C(13)—C(17)—C(20)
O(10)—C(5)—C(6)—C(7)	0.1(3)		−164.38(17)
C(4)—C(5)—C(6)—C(7)	−177.57(18)	C(12)—C(13)—C(17)—C(16)
C(5)—C(6)—C(7)—C(8)	179.9(2)		−153.88(17)
C(6)—C(7)—C(8)—C(9)	0.6(4)	C(18)—C(13)—C(17)—C(16)	78.17(19)
C(6)—C(7)—C(8)—C(14)	−176.76(18)	C(14)—C(13)—C(17)—C(16)	−39.08(18)
C(7)—C(8)—C(9)—C(11)	132.1(2)	C(15)—C(16)—C(17)—C(20)	148.70(17)
C(14)—C(8)—C(9)—C(11)	−50.3(2)	C(15)—C(16)—C(17)—C(13)	17.7(2)
C(6)—C(5)—C(10)—C(19)	55.8(3)	C(13)—C(17)—C(20)—C(22)
C(4)—C(5)—C(10)—C(19)	−126.3(2)		−177.80(17)
C(6)—C(5)—C(10)—C(1)	−125.7(2)	O(16)—C(17)—C(20)—C(22)	60.4(2)
C(4)—C(5)—C(10)—C(1)	52.1(2)	O(13)—C(17)—C(20)—C(21)	−55.2(2)
O(1)—C(1)—C(10)—C(19)	5.6(3)	O(16)—C(17)—C(20)—C(21)
C(2)—C(1)—C(10)—C(19)	125.6(2)		−176.91(17)
O(1)—C(1)—C(10)—C(5)	−172.83(15)	C(21)—C(20)—C(22)—C(23)	116.8(2)
C(2)—C(1)—C(10)—C(5)	−52.9(2)	O(17)—C(20)—C(22)—C(23)	−117.7(2)
C(8)—C(9)—C(11)—C(12)	50.6(3)	C(20)—C(22)—C(23)—C(24)	177.65(18)
C(9)—C(11)—C(12)—C(13)	−54.9(3)	C(22)—C(23)—C(24)—O(3)	117.2(2)
C(11)—C(12)—C(13)—C(18)	−65.8(2)	C(22)—C(23)—C(24)—C(28)	−2.8(3)
O(11)—C(12)—C(13)—C(14)	56.4(2)	C(22)—C(23)—C(24)—C(25)	−129.9(2)
C(11)—C(12)—C(13)—C(17)	166.37(17)	O(3)—C(24)—C(25)—C(26)	−53.6(2)
C(7)—C(8)—C(14)—C(15)	−2.1(3)	C(28)—C(24)—C(25)—C(26)	65.2(2)
C(9)—C(8)—C(14)—C(15)	−179.81(19)	C(23)—C(24)—C(25)—C(26)
C(7)—C(8)—C(14)—C(13)	−126.6(2)		−167.32(18)
C(9)—C(8)—C(14)—C(13)	55.7(2)	O(3)—C(24)—C(25)—C(27)	−179.52(17)
O(12)—C(13)—C(14)—C(8)	−58.2(2)	C(28)—C(24)—C(25)—C(27)	−60.8(2)
O(18)—C(13)—C(14)—C(8)	63.9(2)	C(23)—C(24)—C(25)—C(27)	66.7(2)
O(17)—C(13)—C(14)—C(8)	−179.21(17)

TABLE 7


Hydrogen bonds for 1α,24(S)-dihydroxyvitamin D₂[Å and °].

D-H...A	d(D-H)	d(H...A)	d(D...A)	<(DHA)

O(1)—H(1O)...O(1S)	0.94	1.79	2.714(7)	169.7
O(1)—H(1O)...O(1S′)	0.94	1.82	2.715(7)	159.1
O(2)—H(2O)...O(3)#1	0.99	1.77	2.7009(18)	154.8
O(3)—H(3O)...O(1)#2	0.93	1.88	2.764(2)	158.0
O(1S)—H(1S)...O(2)#3	0.84	1.96	2.783(7)	167.7
O(1S′)—H(1S′)...O(2)#3	0.84	1.99	2.759(6)	151.7

Claims

I claim:

1. 1α,24(S)-dihydroxyvitamin D₂in crystalline form.

2. The three dimensional structure for 1α,24(S)-dihydroxyvitamin D₂as illustrated in FIG. 6 herein and as defined by the atomic positional parameters set forth in Tables 1-7 herein.

3. A method of purifying 1α,24(S)-dihydroxyvitamin D₂, comprising the steps of:

(a) crystallizing 1α,24(S)-dihydroxyvitamin D₂from a solvent; and

(b) recovering the crystallized 1α,24(S)-dihydroxyvitamin D₂.

4. The method of

claim 3

wherein said solvent is a binary system selected from the group consisting of an acetone and hexane mixture, a 2-propanol and hexane mixture, and an ethyl formate and petroleum ether mixture.

5. The method of

claim 3

wherein said solvent comprises a binary system including acetone and hexane, and further including the steps of boiling said acetone, dissolving a product containing 1α,24(S)-dihydroxyvitamin D₂in said boiling acetone, and thereafter adding said hexane to said boiling acetone containing said 1α,24(S)-dhydroxyvitmain D₂prior to crystallizing the 1α,24(S)-dihydroxyvitamin D₂.

6. The method of

claim 3

wherein said solvent comprises a binary system including 2-propanol and hexane, and further including the steps of boiling a mixture of 2-propanol and hexane and dissolving a product containing 1α,24(S)-dihydroxyvitamin D₂in said boiling mixture prior to crystallizing the 1α,24-dihydroxyvitamin D₂.

7. The method of

claim 3

wherein said solvent comprises a binary system including ethyl formate and petroleum ether, and further including the steps of boiling said ethyl formate, dissolving a product containing 1α,24(S)-dihydroxyvitamin D₂in said boiling ethyl formate, and thereafter adding said petroleum ether to said boiling ethyl formate containing said 1α,24(S)-dihydroxyvitamin D₂prior to crystallizing the 1α,24(S)-dihydroxyvitamin D₂.

8. The method of

claim 3

wherein the step of recovering comprises filtering.

9. The method of

claim 3

further including the step of (c) repeating steps (a) and (b) using the recovered crystals from step (b).

10. A method of purifying 1α,24(S)-dihydroxyvitamin D₂, comprising the steps of:

(a) boiling acetone under inert atmosphere;

(b) dissolving a product containing 1α,24(S)-dihydroxvitamin D₂to be purified in said boiling acetone to form a solution;

(c) adding hexane to said solution;

(d) cooling said solution below ambient temperature for a sufficient amount of time to form a precipitate of 1α,24(S)-dihydroxyvitamin D₂crystals, and

(e) recovering the 1α,24(S)-dihydroxyvitamin D₂crystals.

11. The method of

claim 10

further including the step of allowing said solution to cool to ambient temperature prior to cooling below ambient temperature.

12. The method of

claim 10

wherein said inert atmosphere is an argon atmosphere.

13. The method of

claim 10

wherein said solution is cooled to between about 35° F. to about 45° F.

14. The method of

claim 10

wherein the step of recovering comprises filtering.

15. The method of

claim 10

further including the step of (f) repeating steps (a) through (e) using the recovered crystals from step (e) as the product of step (b).

16. A method of purifying 1α,24(S)-dihydroxyvitamin D₂, comprising the steps of:

(a) boiling 2-propanol-hexane mixture under inert atmosphere;

(b) dissolving a product containing 1α,24(S)-dihydroxyvitamin D₂to be purified in said mixture to form a solution;

(c) cooling said solution below ambient temperature for a sufficient amount of time to form a precipitate of 1α,24(S)-dihydroxyvitamin D₂crystals, and

(d) recovering the 1α,24(S)-dihydroxyvitamin D₂crystals.

17. The method of

claim 16

18. The method of

claim 16

wherein said inert atmosphere is an argon atmosphere.

19. The method of

claim 16

wherein said solution is cooled to between about 35° F. to about 45° F.

20. The method of

claim 16

wherein the step of recovering comprises filtering.

21. The method of

claim 16

further including the step of (e) repeating steps (a) through (d) using the recovered crystals from step (d) as the product of step (b).

22. A method of purifying 1α,24(S)-dihydroxyvitamin D₂, comprising the steps of:

(a) boiling ethyl formate under inert atmosphere;

(b) dissolving a product containing 1α,24(S)-dihydroxyvitamin D₂to be purified in said boiling ethyl formate to form a solution;

(c) adding petroleum ether to said solution;

(d) cooling said solution below ambient temperature for a sufficient amount of time to form a precipitate of 1α,24(S)-dihydroxyvitamin D₂crystals; and

(e) recovering the 1α,24(S)-dihydroxyvitamin D₂crystals.

23. The method of

claim 22

24. The method of

claim 22

wherein said inert atmosphere is an argon atmosphere.

25. The method of

claim 22

wherein said solution is cooled to between about 35° F. to about 45° F.

26. The method

claim 22

wherein the step of recovering comprises filtering.

27. The method of

claim 22