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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443511Generated: October 30, 2026

2-(1-Ethoxycarbonyl-2-vinyl-cyclopropylcarbamoyl)-4-[2-(3,5-difluoro-phenyl)-7-methoxy-8-methyl-quinazolin-4-yloxy]-cyclopentanecarboxylic acid → 1-{[4-[2-(3,5-Difluoro-phenyl)-7-methoxy-8-methyl-quinazolin-4-yloxy]-2-(hex-5-enyl-methyl-carbamoyl)-cyclopentanecarbonyl]-amino}-2-vinyl-cyclopropane-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1443511

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(1-Ethoxycarbonyl-2-vinyl-cyclopropylcarbamoyl)-4-[2-(3,5-difluoro-phenyl)-7-methoxy-8-methyl-quinazolin-4-yloxy]-cyclopentanecarboxylic acidHCID 68410387—
ReactantN-Methylhex-5-en-1-amine hydrochlorideHCID 71413963—
Product1-{[4-[2-(3,5-Difluoro-phenyl)-7-methoxy-8-methyl-quinazolin-4-yloxy]-2-(hex-5-enyl-methyl-carbamoyl)-cyclopentanecarbonyl]-amino}-2-vinyl-cyclopropane-carboxylic acid ethyl esterHCID 6841307981%

Reaction Steps

The acid 167 was reacted with hex-5-enyl-methyl-amine hydrochloride as according to the same procedure described in example 157, which gave the title compound (0.838 g, 81%), LRMS (M+H) 691.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659245B2
Source datasetuspto-grants-2010_02
ORD IDord-08cb3c2ae77a402986b6eaa5fa49a6fb
Source noteuspto-grants-2010_02