A kind of cyclic aminopyrimidine derivative and its activity and application of inhibiting kinase

A technology of aminopyrimidine and derivatives, applied in the field of medicine, has achieved great clinical application value, novel synthetic route, and good production feasibility

Active Publication Date: 2021-08-27
HANGZHOU BIO CREATIVITY PHARM TECH CO LTD
View PDF7 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0021] Although there are many reports of macrocyclic compounds in pan-CDKs activity, the structure that selectively inhibits CDK4 / 6 activity has not been reported. Based on this, we designed a new type of macrocyclic structure that can selectively inhibit CDK4 / 6

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
  • A kind of cyclic aminopyrimidine derivative and its activity and application of inhibiting kinase
  • A kind of cyclic aminopyrimidine derivative and its activity and application of inhibiting kinase
  • A kind of cyclic aminopyrimidine derivative and its activity and application of inhibiting kinase

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0067] Synthesis of compound T-1.

[0068]

[0069] Compound T-1: ( E )-4 4 -((4-Ethylpiperazin-1-yl)methyl)-1 4 ,2 5 -difluoro-1 2 -Methyl-1 1 H -5-Oxa-3-aza-1(6,1)-benzo[ d ]imidazole-2(4,2)-pyrimidine-4(1,3)-benzocycloundec-8-ene was synthesized according to the general procedure shown below:

[0070]

[0071]

[0072] Scheme 1 T-1 synthetic route.

[0073] Step 1: 4-(1-(3-buten-1-yl)-4-fluoro-2-methyl-1 H -Benzo[ d ]imidazol-6-yl)-N-(3-(3-butene-1-oxyl)-4-((4-ethylpiperazin-1-yl)methyl)phenyl)-5-fluoro Synthesis of pyrimidin-2-amine (1).

[0074] Intermediate Z-1 (0.27 g, 0.8 mmol), W1-1 (0.29 g, 1.0 mmol), cesium carbonate (0.52 g, 1.6 mmol), 4,5-bisdiphenylphosphine-9,9-dimethyl Xanthoxanthene (Xantphos, 0.093 g, 0.16 mmol) was dissolved in 10 mL of 1,4-dioxane, nitrogen was replaced three times, and Pd was added 2 (dba) 3 , heated to 90°C for 3 hours, poured the reaction solution into 30 mL water and extracted with ethyl acetate (20 mL x 2), com...

Embodiment 3

[0114] Synthesis of Compound T-3.

[0115]

[0116] Compound T-3: ( E )-4 5 -((4-Ethylpiperazin-1-yl)methyl)-1 4 ,2 5 -difluoro-1 2 -Methyl-1 1 H -5-oxa-3-aza-1 (6, 1)-benzo[d]imidazole-2 (4, 2)-pyrimidine-4 (2, 4)-pyridocycloundecane-8- Alkenes are shown as follows:

[0117] .

[0118] Referring to the synthesis method of Example 1, a yellow solid T-3 was obtained, MS (m / z): 561.3 [M+H] + .

[0119] Synthetic route of side chain W3-1:

[0120]

[0121] Step 1: Synthesis of (4,6-dichloropyridin-3-yl)(4-ethylpiperazin-1-yl)methanone (22).

[0122] 4,6-Dichloronicotinic acid (21, 3.8 g, 20 mmol) was dissolved in 100 mL toluene, added 3 mL thionyl chloride, reacted at 100°C for 5 hours, spin-dried the solvent, dissolved in DCM, -10°C Add ethylpiperazine (13, 2.3 g, 20 mmol) and triethylamine (2.0 g, 20 mmol) dropwise to the DCM reaction liquid under the conditions, react for 1 hour, spin to dry the solvent, dissolve in 50 mL EA, and wash with saturated bri...

Embodiment 4

[0134] Synthesis of T-27.

[0135]

[0136] Compound T-27: (1 3 Z ,1 4 E ,10 E )--1 7 ,2 5 -Difluoro-1 2 -Methyl-4 4 -((4-Ethylpiperazin-1-yl)-methyl-)-1 2 H -5-oxa-3-aza-1(5,3)-indazole-2(4,2)-pyrimidine-4(1,3)-benzocyclododec-10-ene is as follows The general operation shown is synthetic:

[0137]

[0138] Synthetic route of Scheme 8 T-27.

[0139] step 1:( E )-N-(3-((6-bromo-5-hexen-1-yl)oxy) 4-((4-ethylpiperazin-1-yl)methyl)phenyl)-5-fluoro -4-(7-fluoro-3-iodo-2-methyl-2 H -Synthesis of indazol-5-yl)pyrimidin-2-amine (27).

[0140] Intermediate Z-2 (0.32 g, 0.8 mmol), W1-2 (0.4 g, 1.0 mmol), cesium carbonate (0.52 g, 1.6 mmol), Xantphos (0.093 g, 0.16 mmol) were dissolved in 10 mL of 1,4- In dioxane, replace nitrogen three times, add Pd 2 (dba) 3 , heated to 90°C and reacted for 3 hours, poured the reaction solution into 30 mL water and extracted with ethyl acetate (20 mLx 2), combined the organic phases, washed with saturated brine, dried over a...

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

PropertyMeasurementUnit
strengthaaaaaaaaaa
Login to view more

Abstract

A cyclic aminopyrimidine derivative and its activity and application for inhibiting kinase The derivative can inhibit the activity of kinases, is a variety of kinase inhibitors, can be more widely used in the treatment of cancer, and has great clinical application prospects. General formula (I).

Description

technical field [0001] The invention belongs to the technical field of medicine, and relates to a cyclic aminopyrimidine derivative and its inhibitory effect on kinases, and also includes a preparation method of the derivative and a pharmaceutically acceptable salt, ester or solvate, and is a variety of kinase inhibitors , has the purpose of treating cancer, and has a huge application prospect. Background technique [0002] Cancer is still the number one killer of human health. According to the statistics of the National Institutes of Health (NIH), in 2012, there were 14.1 million new cases worldwide and 8.2 million cancer-related deaths. In 2012, 57% of new cancer cases occurred in less developed regions of the world, including Central America and Africa and parts of Asia, and 65% of cancer deaths also occurred in these regions. In 2018 alone, there were more than 1.7 million new cancer cases, and by 2030, the number of new cancer cases is expected to increase to 23.6 mill...

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 Patents(China)
IPC IPC(8): C07D498/18C07D498/22A61P35/00A61P35/02
CPCA61P35/00A61P35/02C07D498/18C07D498/22
Inventor 盛荣张冯敏罗瑾吴立军杨欢金泽武熊晓红钱扬
Owner HANGZHOU BIO CREATIVITY PHARM TECH CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

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

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap