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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481136Generated: October 26, 2026

Cyanogen Bromide → Quinazolin-2-amine

https://huagongshe.com/reaction/481136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHydrate;hydrochlorideHCID 21885828—
Reactantethyl-N-(6-amino-2,3-dichlorobenzyl)glycineHCID 67080112—
ReactantAnagrelideHCID 135409400—
ProductQuinazolin-2-amineHCID 178508286—

Reaction Steps

Commercially, as discussed in U.S. Pat. No. 5,801,245 and as shown in FIG. 1, Anagrelide has been prepared as the hydrochloride monohydrate (compound IV) from the intermediate, ethyl N-(6-amino-2,3-dichlorobenzyl)glycine (compound I) by reaction with cyanogen bromide in hot alcohol solution, or, preferentially, by reaction with cyanogen bromide in an aprotic solvent to give the iminoquinazoline intermediate (compound II) which is isolated and then reacted with a base in a hot solution of alcohol to form Anagrelide base (compound III).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06653500B2
Source datasetuspto-grants-2003_11
ORD IDord-cfab49f40e6e4e44a0f2973c0270664c
Source noteuspto-grants-2003_11