Name | (E|Z)-3α-hydroxy-6-ethylidene-7-keto-5β-cholan-24-oic acid Methyl ester |
Synonyms | N-3 OB-4 Obeticholic Acid inter. OB-4 (3alpha,5beta)-6-Ethylidene-3-hydroxy-7-oxocholan-24-oic acid methyl ester |
CAS | 863239-59-2 |
Molecular Formula | C27H42O4 |
Molar Mass | 430.61998 |
Boling Point | 534.3±43.0 °C |
CN201710202448.5
date of application:
2017-03-30
public/announcement number:
CN106916196A
date of publication/announcement:
2017.07.04
Applicant (patentee):
chengdu lvlin technology co., ltd
Inventor:
Liang zhengquan , yellow pine , Dong Qiang ,< a href = "https://xueshu.baidu.com/s?wd=author: (Zhou Cai'e) & tn = SE_baiduxueshu_c1gjeupa & ie = utf-8 & SC _f_para = SC _hilight = person" target = "_blank"> Zhou Cai'e
national and provincial code:
CN510112
Summary:
The present invention discloses a synthesis method of the intermediate of Obeticholic acid, using sodium bromide, sulfuric acid and sodium bromate solution as raw materials, the oxidation of chenodeoxycholic acid to 3α hydroxyl 7 ketone group 5 beta choline acid (I). In order to solve the problems of cumbersome post-treatment, long treatment time and low yield in the synthesis of the existing 3α hydroxyl 7 ketone 5 β cholanic acid (I) industry, the synthesis method provided by the present invention reduces the controllable cost in the production process, reduces the cumbersome operation and safety problems, is conducive to industrial production, and is conducive to further improving the yield and quality of oberacholic acid, reducing production costs, and improving, reduce impurity content.
patent for invention
application (patent) number:
CN201611203526.5
date of application:
20161223
public/announcement number:
CN108239134A
date of publication/announcement:
20180703
Applicant (patentee):
Shanghai bobang pharmaceutical technology co., ltd
Inventor:
Gao Heyong ,< a href = "https://xueshu.baidu.com/s?wd=author: (Liu Shengquan) & tn = SE_baiduxueshu_c1gjeupa & ie = utf-8 & SC _f_para = SC _hilight = person" target = "_blank"> Liu Shengquan ,< a href = "https://xueshu.baidu.com/s?wd=author: (Bi Pengfei) & tn = SE_baiduxueshu_c1gjeupa & ie = utf-8 & SC _f_para = SC _hilight = person" target = "_blank"> Bi Pengfei , Sun Bingyang , Liu Zhende
national and provincial code:
CN310115
Summary:
The present invention discloses an auticholic acid intermediate and a preparation method and application thereof. The intermediate has the chemical structure shown in Formula III and Formula IV respectively: the use of the intermediate of the present invention to synthesize auticholic acid has the advantages of high total molar yield, simple operation, high three-dimensional selectivity, safety and no pollution, no special requirements for equipment, low production cost, etc., and has strong practical value for realizing the industrialization of auti, significant progress compared to the existing technology.
patent for invention
application (patent) number:
CN202011624507.6
date of application:
20201230
public/announcement number:
CN112724187A
date of publication/announcement:
20210430
Applicant (patentee):
Nanjing youjie pharmaceutical technology co., ltd
Inventor:
fu mingwei , Wang Huaiqiu , Xiao Ya
national and provincial code:
CN320106
Summary:
The present invention discloses a method for continuous hydrogenation of a fixed bed to prepare an Obeticholic acid intermediate. The Obeticholic acid intermediate 1 is reacted with hydrogen in a fixed bed reactor filled with a catalyst; the structural formula of the Obeticholic acid intermediate 1 is shown in (I); the catalyst is palladium/carbon, palladium/aluminum oxide, platinum/carbon, one or more mixtures of platinum/aluminum trioxide or nickel/silica; the present invention not only has fast reaction speed, high conversion rate, simple and safe operation process, but also has low cost, can be carried out continuously, and can reduce the problem of three wastes.