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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518676Generated: November 1, 2026

Cyanogen Bromide → HCID 178491277, compound

https://huagongshe.com/reaction/518676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 178491294HCID 178491294—
SolventEthanolHCID 702—
ProductHCID 178491277HCID 17849127799.9%

Reaction Steps

To a solution of cis-4-(2-amino-5-(4-methoxybenzyloxy)phenylamino)-N-isopropylcyclohexanecarboxamide (400 mg, 0.972 mmol) in EtOH (4.8 mL) was added cyanic bromide (165 mg, 1.555 mmol) and the mixture was stirred at RT for 2 hours. The solvent was evaporated, and the residue was diluted with DCM (about 10 mL), washed with water, 1N aqueous NaOH, and brine. The organic layer was dried over Na2SO4, filtered and the solvent was removed to afford cis-4-(2-amino-6-(4-methoxybenzyloxy)-1H-benzo[d]imidazol-1-yl)-N-isopropylcyclohexanecarboxamide (424 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115127B2
Source datasetuspto-grants-2015_08
ORD IDord-87cabf17fad04992a1b5bbb6d5effb5f
Source noteuspto-grants-2015_08