Method for preparing vitamin D3 analogue intermediate

A technology of intermediates and analogs, applied in the field of pharmaceutical chemical synthesis, can solve the problems of low selectivity of chiral reduction, difficulty in purification, long reaction steps, etc., to achieve industrial scale production, overcome long reaction time, unit The effect of less operation

Active Publication Date: 2017-06-30
CHONGQING HUABANGSHENGKAI PHARM
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

The whole reaction steps are long, the operation is cumbersome, there are many impurities, which are difficult to remove, and the yield is low, and the third and eighth deprotection selectivity is not high, and the sixth step chiral reduc

Method used

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  • Method for preparing vitamin D3 analogue intermediate
  • Method for preparing vitamin D3 analogue intermediate
  • Method for preparing vitamin D3 analogue intermediate

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] The preparation of embodiment 1 intermediate IV

[0044]Under nitrogen protection, compound II (26.9g, 129.3mmol) was added to a 1000ml three-neck flask, raw material III (45.9g, 194.0mmol), tetrahydrofuran (300ml) was added, stirred evenly, cooled to -50°C, and the reaction was stirred for 2-3 Hours, after HPLC detects that the reaction is complete, the reaction solution is poured into ice water, stirred for 0.5-1.0 hours, the solution is extracted with n-hexane (200ml×3), washed with methanol:water=3:1 (50ml×3), and depressurized The solvent was distilled off to obtain 28.0 g of oil, with a yield of 78.4% and an HPLC purity of 96.7%.

[0045] The HPLC instrument and detection conditions are as follows:

[0046] Chromatographic column: Agilent ZORBAX SIL, 250×4.6mm, 5μm;

[0047] Mobile phase: n-hexane: isopropanol = 98:2, detection wavelength: 200nm;

[0048] Column temperature: 25°C, injection volume: 20μl, flow rate: 1.0ml / min.

Embodiment 2

[0049] Example 2 Vitamin D 3 Preparation of analog intermediate V

[0050] Add compound IV (52g, 188mmol), catalyst imidazole (23g, 338mmol) and 1000mL dichloromethane into a 250ml three-necked flask. After stirring evenly, add tert-butyldimethylsilyl chloride (42.1g, 280mmol) in three batches, After the addition is complete, react at room temperature for 2-2.5 hours. After the reaction is detected by TLC (developing agent n-hexane:ethyl acetate=10:1, Rf of IV=0.4, Rf of V=0.6), add 100ml of water to wash , liquid separation, the organic phase was washed with 100ml of water × 2, the organic phase was collected, dried over anhydrous sodium sulfate, filtered, and distilled under reduced pressure until no fraction flowed out to obtain oily vitamin D 3 The analog intermediate V was 62.5g, the yield was 85.1%, and the HPLC purity was 95.9%.

[0051] The HPLC instrument and detection conditions are as follows:

[0052] Chromatographic column: Agilent ZORBAX SIL, 250×4.6mm, 5μm; ...

Embodiment 3

[0055] Example 3 Vitamin D 3 Preparation of analog intermediate V

[0056] The compound represented by formula I in this embodiment can be obtained through commercial channels, and can also be obtained from vitamin D 2 Obtained by ozonation reduction reaction. Vitamin D 2 For the preparation of the compound represented by formula I by ozonation, reference can be made to document US20130006003.

[0057] (1) with vitamin D 2 Preparation of compound I

[0058] 400g Vitamin D 2 Dissolved in 4L of dichloromethane and 12L of methanol, the solution was cooled to -70°C, passed through ozone until the solution turned blue, the obtained ozonide was reduced with 308g of sodium borohydride, then washed with saturated brine, the organic layer was concentrated, and then passed through the column, Concentrate and dry to obtain 148g of compound I with a yield of 68%.

[0059] (2) Prepare compound II with compound I

[0060] Add compound I (26.1g, 123.1mmol) and dichloromethane (300ml)...

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Abstract

The invention belongs to the technical field of drug chemical synthesis, and particularly relates to a method for preparing a vitamin D3 analogue intermediate, specifically relating to a method for preparing calcipotriol intermediate. The method comprises the following steps: performing WITTIG-HORER reaction to a compound shown in the formula II with raw materials shown in the formula III, to obtain an intermediate shown in the formula IV; performing hydroxyl protection reaction to the intermediate shown in the formula IV, to obtain the vitamin D3 analogue intermediate shown in the formula V. The method has fewer steps and fewer unit operations, the yield is high, and the total yield is up to 40% above, and the cost is low; isomers are fewer, so that impurities are easily removed, purification is easy, the purity of the intermediate V is up to 95%, the long reaction time, low yield, more impurities and high cost problems in the prior art can be overcome, and the industrial large-scale production is facilitated.

Description

technical field [0001] The invention belongs to the technical field of pharmaceutical chemical synthesis, in particular to a method for preparing vitamin D 3 The method for analog intermediates, in particular relates to a method for preparing calcipotriol intermediates. Background technique [0002] Calcipotriol (MC903) belongs to non-corticosteroid drugs and is vitamin D 3 Active metabolite 1,25-(OH) 2 -D 3 (ie Calcitriol, calcitriol) analogs. Calcipotriol has the effect of inhibiting the proliferation of epidermal keratinocytes and inducing their differentiation, and has also shown its efficacy in treating psoriasis in many clinical trials. The structure of calcipotriol is relatively complex. The structural formula is as follows. It has 7 chiral centers and three alcoholic hydroxyl groups. It is very soluble in 96% alcohol, but very insoluble in water. Calcipotriol is sensitive to light and heat, easy to Deterioration, so the preparation is extremely difficult. [00...

Claims

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Application Information

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IPC IPC(8): C07F7/18
CPCC07C45/29C07C45/68C07F7/1804C07C49/513C07C49/523Y02P20/55
Inventor 邓青均李伦唐朝军
Owner CHONGQING HUABANGSHENGKAI PHARM
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