Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472729Generated: October 25, 2026

Cyclopentylamine → N-(5-Chloro-2,4-dimethoxy-phenyl)-2-{2,4-dioxo-3-[4-(phenethylcarbamoyl-methyl)-phenyl]-3,4-dihydro-2H-quinazolin-1-yl}-acetamide

https://huagongshe.com/reaction/472729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentylamineHCID 2906—
Reactant5-Chloro-2,4-dimethoxyanilineHCID 66807—
Reactant{1-[(5-Chloro-2,4-dimethoxy-phenylcarbamoyl)-methyl]-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl}-acetic acidHCID 24896589—
Reactant{2,4-dioxo-3-[4-(phenethylcarbamoyl-methyl)-phenyl]-3,4-dihydro-2H-quinazolin-1-yl}-acetic acidHCID 68588311—
ProductN-(5-Chloro-2,4-dimethoxy-phenyl)-2-{2,4-dioxo-3-[4-(phenethylcarbamoyl-methyl)-phenyl]-3,4-dihydro-2H-quinazolin-1-yl}-acetamideHCID 59317686—

Reaction Steps

This compound is made analogously to Example 1-2 by replacing {1-[(5-chloro-2,4-dimethoxy-phenylcarbamoyl)-methyl]-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl}-acetic acid (Intermediate A) with ({2,4-dioxo-3-[4-(phenethylcarbamoyl-methyl)-phenyl]-3,4-dihydro-2H-quinazolin-1-yl}-acetic acid) (Intermediate D) and by replacing cyclopentylamine with 5-chloro-2,4-dimethoxy-phenylamine to afford the title compound. The reaction is carried out using DMF as the solvent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633211B2
Source datasetuspto-grants-2014_01
ORD IDord-3a4e43596d004d088cc977bdaf72d118
Source noteuspto-grants-2014_01