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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361902Generated: October 30, 2026

Cyanogen Bromide → HCID 178473435, compound

https://huagongshe.com/reaction/2361902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 418338HCID 418338—
SolventEthanolHCID 702—
ProductHCID 178473435HCID 17847343538%

Reaction Steps

Cyanogen bromide (0.55 g, 5.2 mmol) was added to a stirred solution of ethyl 5,6-diamino-4-chloro-2-pyridinecarbamate (intermediate for the preparation of 1, 1.00 g, 4.3 mmol) in 20 mL of ethanol at room temperature. The solution was stirred for 3 h and then at 60° C. for 3 h. The precipitate was filtered and washed with diethyl ether to give (2-amino-7-chloro-3H-imidazo[4,5-b]pyridin-5-yl)-carbamic acid ethyl ester (0.55 g, 38%) as a yellow powder. 1H NMR confirmed the structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691814B2
Source datasetuspto-grants-2014_04
ORD IDord-34c4b74cf9af4e41b0214fc7e8d838dc
Source noteuspto-grants-2014_04