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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178727Generated: October 26, 2026

Cyanogen Bromide → Quinazolin-2-amine

https://huagongshe.com/reaction/2178727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHydrate;hydrochlorideHCID 21885828—
Reactantethyl-N-(6-amino-2,3-dichlorobenzyl)glycineHCID 67080112—
ReactantAnagrelideHCID 135409400—
SolventTolueneHCID 1140—
ProductQuinazolin-2-amineHCID 178508286—

Reaction Steps

Commercially, as discussed in U.S. Pat. No. 5,801,245, and as shown in Scheme 1 below, anagrelide has been prepared as the hydrochloride monohydrate (compound IV) from the intermediate, ethyl-N-(6-amino-2,3-dichlorobenzyl)glycine (compound I), either by reaction with cyanogen bromide in hot alcoholic solution, or, preferentially, by reaction with cyanogen bromide in an aprotic solvent such as toluene 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 numberUS09067944B2
Source datasetuspto-grants-2015_06
ORD IDord-1ab8ad0e7f384b0191570b857b431b25
Source noteuspto-grants-2015_06