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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388991Generated: October 30, 2026

Cyanogen Bromide → HCID 178480620, compound

https://huagongshe.com/reaction/388991

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 numberUS08377983B2
Source datasetuspto-grants-2013_02
ORD IDord-b6644d2e5a7148e2822e217ac973009d
Source noteuspto-grants-2013_02