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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518739Generated: October 29, 2026

Cyanogen Bromide → HCID 178457825, compound

https://huagongshe.com/reaction/518739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 178457842HCID 178457842—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 178457825HCID 17845782562.3%

Reaction Steps

The cis-4-(2-amino-5-morpholinophenylamino)-N-isopropylcyclohexanecarboxamide (315 mg, 0.874 mmol) was dissolved in EtOH (5 mL), and cyanogen bromide (139 mg, 1.311 mmol) was added. The reaction was stirred at RT. After 16 hours, the reaction was diluted with DCM (50 mL) and washed with 1 N aqueous NaOH. The organic layer was concentrated to provide cis-4-(2-amino-6-morpholino-1H-benzo[d]imidazol-1-yl)-N-isopropylcyclohexanecarboxamide as a light purple solid (210 mg, 62.3% yield). MS, m/z (C21H31N5O2): calcd, 385.2. found, 385.8 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115127B2
Source datasetuspto-grants-2015_08
ORD IDord-995a1d793f3d4b1c8475c2131aa9958b
Source noteuspto-grants-2015_08