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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935669Generated: October 26, 2026

Cyanogen Bromide → Quinazolin-2-amine

https://huagongshe.com/reaction/1935669

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 numberUS06388073B1
Source datasetuspto-grants-2002_05
ORD IDord-8a2f6eca11644f39bb21afa3dcb925e5
Source noteuspto-grants-2002_05