Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Preparation method for eldecalcitol intermediate

A saponification and compound technology, applied in the field of preparation of alcalcidol intermediate 1A, can solve the problems of low utilization rate of raw materials, affect product quality, increase the dosage of other materials and reagents, etc., and achieve easy industrial scale-up and improved raw material utilization. rate effect

Active Publication Date: 2015-06-17
SHANGHAI HAOYUAN MEDCHEMEXPRESS CO LTD +1
View PDF3 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0011] Since 1A and 1B do not go through the separation process in the synthetic route but are converted into the key A ring fragment compound 3 or 5 and then separated, there are inevitable defects in these two routes: 1. Due to the existence of compound 1B , resulting in a low utilization rate of raw materials; 2. Since 1B will also participate in the corresponding reaction to prepare compound 3 or 5, it will inevitably increase the workload of the preparation reaction, and at the same time increase the consumption of other materials and reagents; 3. Due to The separation step is placed at the end, and the residue of the diastereoisomer of the key A ring fragment compound 3 or 5 produced by compound 1B is bound to affect the quality of the final product
However, there is no corresponding literature report on the separation of compounds 1A and 1B, only the separation of isomers with different chiral structures

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Preparation method for eldecalcitol intermediate
  • Preparation method for eldecalcitol intermediate
  • Preparation method for eldecalcitol intermediate

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0035] Example 1 Preparation of Compounds 1A and 7 Using Compound 1 as a Raw Material

[0036]

[0037]Dissolve compound 1 (33g, 100mmol) and ethyl acrylate (20g, 200mmol) in 500mL of n-hexane, add Novozyme lipase 4353g at room temperature, heat to 70°C, keep the temperature and react overnight, sample and filter for HPLC detection, 1B Less than 3%, the reaction is complete. The solid was removed by filtration, the filter cake was washed with 200 mL of n-hexane, and the filtrate was collected and concentrated to obtain 35 g of crude product. The crude product was subjected to silica gel column chromatography to obtain 17g of compound 1A with a yield of 52% and a purity of 97%, and compound 716g with a yield of 48% and a purity of 95%.

[0038] Compound 1A: 1H NMR (400MHz, CDCl3) δ = 5.93 (ddd, 1H, J = 17.4, 10.7, 6.2Hz), 5.34 (dt, 1H, J = 17.4, 1.5Hz), 5.23 (dt, 1H, J = 10.2, 1.5Hz), 4.29–4.09(m, 4H), 4.00(dd, 1H, J=8.4, 6.3Hz), 3.79–3.65(m, 3H), 3.30(dd, 2H, J=6.0, 5.0Hz...

Embodiment 2

[0042] The preparation of embodiment 2 compound 1B

[0043]

[0044] Compound 7 (15g, 40.3mmol) was dissolved in 100mL tetrahydrofuran and 100mL methanol, and potassium carbonate (11.1g, 80.6mmol) was added after cooling down to zero. After the addition, the temperature was naturally raised to room temperature for 3 hours. React until the spots of raw materials detected by TLC disappear, and the reaction is complete. The reaction was quenched by adding 300 mL of water. Extracted three times with 100 mL of ethyl acetate, combined the organic phases, washed with 200 mL of saturated brine, dried with 200 g of anhydrous Na2SO4, and concentrated to obtain 14 g of crude product. The crude product was subjected to silica gel column chromatography to obtain 12.5 g of compound 1B with a yield of 93.9% and a purity of 95%.

[0045] 1B: 1H NMR (400MHz, CDCl3) δ = 5.89 (ddd, 1H, J = 17.4, 10.7, 6.2Hz), 5.35 (dt, 1H, J = 17.4, 1.5Hz), 5.24 (dt, 1H, J = 10.2 ,1.5Hz),4.29–4.09(m,4H),4....

Embodiment 3

[0047] The preparation of embodiment 3 compound 8

[0048]

[0049] Compound 1B (10g, 30.4mmol) was dissolved in 100mL of dichloromethane, and Dess Martin oxidant (25.6g, 60.6mmol) was added in batches at zero temperature, and stirred for 3 hours after naturally rising to room temperature. After reacting until the spot of raw material disappeared as observed by TLC, it was quenched by adding 500 mL of n-hexane, filtered, the filter cake was washed with 500 mL of n-hexane, and concentrated to obtain 11 g of crude product. Silica gel column chromatography yielded 89.5 g of the compound, with a yield of 95% and a purity of 93%.

[0050] 8: 1H NMR (400MHz, CDCl3): δ = 6.8-36.74 (1H, m), 6.43-6.37 (1H, dd, J = 1.5, 17.37Hz), 5.80-5.76 (1H, dd, J = 1.5, 10.5 Hz), 4.22-4.17(2H,m), 4.0-3.9(2H,m), 3.79–3.65(m,3H), 3.29(dd,2H,J=6.0,5.0Hz), 2.89(d,1H, J=6.3Hz), 1.92(quint, 2H, J=6.3Hz), 1.42(s, 3H), 1.36(s, 3H), 1.20(s, 9H);

[0051] HRMS(EI)m / z calcd for C17H30O6(M+)328.2048,found...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention relates to a method for preparing a compound 1A through enzymatic resolution. Particularly, a method for enantiomeric separation and recycling comprises the following steps: treating a compound 1 or 9 with enzyme, and obtaining the compound 1A and a compound 7; performing selective saponification, oxidation and reduction on the compound 7 to obtain the compound 1; enabling the obtained compound 1 to enter the steps a-d or a-e again for circulation, thereby achieving purposes of enantiomeric resolution and recycling.

Description

technical field [0001] The present invention relates to a recovery method for enzymatic resolution and separation of racemic compounds and by-products, in particular to a new method for preparing alcalcitol intermediate 1A. Background technique: [0002] Vitamin D (vitamin D) is a sterol derivative with anti-rickets effect, also known as anti-rickets vitamin. At present, it is considered that vitamin D is also a steroid hormone, and the most important members of the vitamin D family are VD2 (ergocalciferol) and VD3 (cholecalciferol). Vitamin D is a derivative of different provitamin D after ultraviolet irradiation. A 40-year study by American scientists found that taking a daily dose of vitamin D can cut the risk of breast, colon and ovarian cancer in half. When the sun shines on the skin, the body produces vitamin D, which accounts for 90% of the body's vitamin D supply. [0003] In recent years, more and more evidence has shown that a lack of vitamin D can be extremely ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C12P41/00C12P17/04
Inventor 丁福斗杨旭慧钱凯敏张宪恕高强郑保富
Owner SHANGHAI HAOYUAN MEDCHEMEXPRESS CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com