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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390206Generated: November 1, 2026

Cyclohexanecarboxylic acid [2-(2-amino-5-benzoyl-benzylamino)-ethyl]-amide → Cyclohexanecarboxylic acid [2-(2-amino-6-benzoyl-4H-quinazolin-3-yl)-ethyl]-amide

https://huagongshe.com/reaction/390206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanecarboxylic acid [2-(2-amino-5-benzoyl-benzylamino)-ethyl]-amideHCID 58625175—
ReactantHCID 178511328HCID 178511328—
SolventEthanolHCID 702—
ProductCyclohexanecarboxylic acid [2-(2-amino-6-benzoyl-4H-quinazolin-3-yl)-ethyl]-amideHCID 58625077—

Reaction Steps

A mixture of cyclohexanecarboxylic acid [2-(2-amino-5-benzoyl-benzylamino)-ethyl]-amide (0.0032 mol) in ethanol (30 mL) was stirred at room temperature. Cyanogen bromine (0.0048 mol) was added. The reaction mixture was stirred and refluxed for 2 hours, then cooled and stirred overnight at room temperature resulting in a precipitate. The precipitate was filtered off, washed with diisopropyl ether and dried to yield the title compound as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383637B2
Source datasetuspto-grants-2013_02
ORD IDord-590fb14c39c246a9b4ede510d42871e4
Source noteuspto-grants-2013_02