Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461329Generated: October 30, 2026

Cyanogen Bromide → 2-(4-Cyanopiperazin-1-yl)-4-amino-6,7-dimethoxyquinazoline

https://huagongshe.com/reaction/461329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
Reactant2-(1-Piperazinyl)-4-amino-6,7-dimethoxyquinazolineHCID 616267—
SolventDimethylformamideHCID 6228—
Product2-(4-Cyanopiperazin-1-yl)-4-amino-6,7-dimethoxyquinazolineHCID 21393366—

Reaction Steps

A mixture of 10.0 g. (0.033 mole) of 2-(1-piperazinyl)-4-amino-6,7-dimethoxyquinazoline, prepared as described in U.S. Pat. No. 3,511,836, 3.54 g. (0.033 mole) of cyanogen bromide and 33 ml. of N,N-dimethylformamide was stirred under nitrogen at room temperature (20°-25° C.) for 6 hours. The precipitated solid was recovered by filtration, washed with ether and air dried to afford 11.6 g. (85%) of the hydrobromide salt of the title compound. The salt was partitioned between 250 ml. of aqueous saturated sodium bicarbonate solution and 500 ml. of chloroform. The layers were separated and the chloroform layer concentrated in vacuo to afford the free base as a dry foam, 8.3 g. (80%); M.P. 215° C. The mass spectrum reveals a molecular ion peak at M/e 314. Infrared spectrum (CHCl3): peak at 4.5 μ (CN).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04062844
Source datasetuspto-grants-1977_12
ORD IDord-0707f2afef084eb4aca41fd75381d8c3
Source noteuspto-grants-1977_12