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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390247Generated: October 30, 2026

Cyanogen Bromide → 3-(2-Amino-6-benzoylquinazolin-3(4H)-YL)-N-cyclohexyl-N-methylpropanamide

https://huagongshe.com/reaction/390247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
Reactant3-(2-Amino-5-benzoyl-benzylamino)-N-cyclohexyl-N-methyl-propionamideHCID 58625111—
SolventEthanolHCID 702—
Product3-(2-Amino-6-benzoylquinazolin-3(4H)-YL)-N-cyclohexyl-N-methylpropanamideHCID 16741238—

Reaction Steps

A mixture of 3-(2-amino-5-benzoyl-benzylamino)-N-cyclohexyl-N-methyl-propionamide (0.017) prepared as described in Example 3 in ethanol (250 mL) was stirred at room temperature and cyanogen bromide (0.027 mol) was added. The reaction mixture was stirred and refluxed for 3 hours, then cooled. The solvent was evaporated and the residue was crystallized from CH3CN. The precipitate was filtered off 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-0055d65aa003494096117b66e2acb368
Source noteuspto-grants-2013_02