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

Preparation method of relugolix drug intermediate

A technique of rilugoli and intermediates, applied in the field of drug synthesis, can solve the problems of high flammability, low flash point, high production environment requirements, etc., and achieve the effect of avoiding substitution reaction

Inactive Publication Date: 2021-02-05
SUZHOU PENGXU PHARM TECH CO LTD
View PDF2 Cites 8 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] The highly toxic substance ethyl chloroformate is used in the synthesis process of the above two disclosed synthetic routes, and has a very low flash point, is highly flammable, and has high requirements for the production environment

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 of relugolix drug intermediate
  • Preparation method of relugolix drug intermediate
  • Preparation method of relugolix drug intermediate

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0021]

[0022] Toluene (450 mL) and compound 1 (150 g) were added in sequence to a 2 L reaction flask, stirring was started, propyl chloroformate (120 g) was added dropwise, and the reaction was heated under reflux for 2 h. Cool down to 50-60 °C, control the internal temperature at 50-60 °C and add ethanol (1350 mL) dropwise. After the dropwise addition, slowly lower the temperature to an internal temperature of 0-10 °C, stir for 1 h, filter, and rinse the filter cake with ethanol (300 mL). Drying in vacuo at 45 °C gave a yellow solid with a yield of 84.4% and a purity of 98%.

[0023] The NMR data of compound 2-a are as follows:

[0024] 1 H NMR (400 MHz, CDCl 3 ) δ 10.67 (s, 1H), 8.31-8.22 (m, 2H), 7.59-7.52 (m,2H), 4.39 (q, J = 7.1 Hz, 2H), 4.21 (t, J = 6.7 Hz, 2H) , 2.42 (s, 3H), 1.80-1.67 (m, 2H), 1.42 (t, J = 7.1 Hz, 3H), 1.00 (t, J = 7.4 Hz, 3H).

Embodiment 2

[0026]

[0027] Add toluene (1.5 mL) and compound 1 (0.5 g) to the 10 mL reaction flask in sequence, start stirring, add isopropyl chloroformate (0.4 g) dropwise, and heat to reflux for 2 h. Cool down to 20-30 °C, add purified water (4 mL) and dichloromethane (4 mL), separate layers, extract the aqueous phase with dichloromethane (4 mL), combine the organic phases, and concentrate under reduced pressure to obtain compound 2 -b The crude product was purified by column (ethyl acetate: n-heptane = 1:10) to obtain 0.58 g of a bright yellow solid with a yield of 90% and a purity of 98%.

[0028] The NMR data of compound 2-b are as follows:

[0029] 1 H NMR (400 MHz, DMSO-d6) δ 10.45 (s, 1H), 8.29 – 8.23 ​​(m, 2H), 7.69 – 7.63 (m, 2H), 5.02 – 4.91 (m, 1H), 4.32 (m, J = 7.1 Hz, 2H), 2.34 (s, 3H), 1.33 (t, J = 7.1 Hz, 3H), 1.29 (d, J = 6.3 Hz, 6H).

Embodiment 3

[0031]

[0032] Add toluene (1.5 mL), compound 1 (0.10 g) in sequence to the 10 mL reaction bottle, add K 2 CO 3 (90 mg), start stirring, add benzyl chloroformate (0.136 g) dropwise, and heat under reflux for 4 h. Cool down to 20-30 °C, add purified water (4 mL) and toluene (4 mL), separate the layers, extract the aqueous phase with toluene (4 mL), combine the organic phases, and concentrate under reduced pressure to obtain the crude compound 2-c. After column purification (ethyl acetate: n-heptane = 1:6), 0.103 mg of a bright yellow solid was obtained, with a yield of 71.5% and a purity of 98%.

[0033] The NMR data of compound 2-c are as follows:

[0034] 1 H NMR (400 MHz, CDCl 3 ) δ 10.75 (s, 1H), 8.37-8.16 (m, 2H), 7.62-7.50 (m,2H), 7.49-7.32 (m, 5H), 5.27 (s, 2H), 4.37 (q, J = 7.1 Hz, 2H), 2.41 (s, 3H), 1.40 (t, J = 7.1 Hz, 3H).

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 provides a relugolix intermediate and a synthesis scheme of relugolix, the synthesis scheme adopted by the invention effectively avoids the use of a high-toxicity substance methyl chloroformate or ethyl chloroformate, and other types of chloroformate which is low in toxicity and convenient to use are adopted, so that the use risk in the production process of crude drugs can be reduced, and the production cost is reduced. Operation is easy, the process is safer, and industrial production is facilitated.

Description

technical field [0001] The application relates to the field of drug synthesis, in particular to a preparation method of a thieno[2,3-d]pyrimidine compound exhibiting gonadotropin-releasing hormone (GnRH) antagonistic activity and an intermediate thereof. Background technique [0002] Endometriosis is caused by the growth of endometrium in any part other than the uterine cavity. It is a common estrogen-dependent gynecological disease that often occurs during women's reproductive years. Its mechanism of action is still unclear. The difficult diagnosis and complex symptoms of endometriosis, such as unknown etiology, have seriously hindered the discovery of effective treatments. At present, endometriosis is mainly diagnosed by laparoscopy and treated by surgery, or by taking contraceptives, GnRH receptor agonists or progestins to reduce estrogen levels in the body to control. In July 2018, Eragolix Sodium, the world's first oral GnRH antagonist in this field, was approved by th...

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): C07D495/04C07D333/38C07D409/12
CPCC07D333/38C07D409/12C07D495/04
Inventor 李丕旭王鹏谷向永高峰葛亚东刘远华
Owner SUZHOU PENGXU PHARM TECH 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