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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614902Generated: October 29, 2026

Cyanogen Bromide → Anagrelide Hydrochloride

https://huagongshe.com/reaction/614902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantEthyl 2-((6-amino-2,3-dichlorobenzyl)amino)acetateHCID 9814186—
Solvent2-MethoxyethanolHCID 8019—
ProductAnagrelide HydrochlorideHCID 13541349431%

Reaction Steps

A solution of cyanogen bromide (3.2 g, 0.030 mol) in 100 ml. 2-methoxyethanol was added to a solution of N-(6-amino-2,3-dichlorobenzyl)glycine ethyl ester (8.2 g, 0.030 mol) in 250 ml. 2-methoxyethanol. The solution was stirred at room temperature for 1 hour, heated at reflux for 22 hours, and cooled. The precipitate was filtered off, washed with ether and air dried to give 3.11 gms. of the crude title product (31% yield as the hydrobromide salt). Recrystallization from ethanolic HCl gave the pure title product in 71% recovery (22% overall yield); m.p. >250°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04146718
Source datasetuspto-grants-1979_03
ORD IDord-56be5e26d86e45a2bf84af2e8d3aedad
Source noteuspto-grants-1979_03