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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163436Generated: October 29, 2026

Cyanogen Bromide → HCID 178480620, compound

https://huagongshe.com/reaction/1163436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 68443410HCID 68443410—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
ProductHCID 178480620HCID 178480620—

Reaction Steps

To a solution of 4,5-diamino-2-(4-methylpiperazin-1-yl)-N-(1H-indazol-6-yl)-benzamide (2 mmol; see Example 181) in 10% aqueous EtOH (6 mL) was added cyanogen bromide (2.2 mmol), and the mixture was heated at reflux for 4 h. The reaction mixture was then concentrated in vacuo, and the residue obtained was suspended in diethyl ether with vigorous stirring. The solid obtained was collected by filtration, washed with diethyl ether, and dried in vacuo to afford 2-amino-6-(4-methylpiperazin-1-yl)-1H-benzimidazole-5-carboxylic acid (1H-indazol-6-yl)-amide as a hydrobromide salt. MS: m/z 391 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820821B2
Source datasetuspto-grants-2010_10
ORD IDord-58b6101319094fdbb9ae75bbb6093257
Source noteuspto-grants-2010_10