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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968799Generated: October 29, 2026

HCID 178418361, compound → HCID 178430523, compound

https://huagongshe.com/reaction/968799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178430969HCID 178430969—
CatalystPlatinumHCID 23939—
SolventDimethylformamideHCID 6228—
ProductHCID 178430523HCID 178430523—

Reaction Steps

A mixture of 7-Methyl-6-nitro-1H-benzimidazole-4-carbonitrile (24) (1.010 g, 5.0 mmol) and Pt/C (5% Pt/C sulfided, 0.502 g, 50 wt %, C5002 Engelhard Industries) in DMF (75 mL) is hydrogenated at about 40 psi hydrogen pressure at about 50° C. over about 24 hours. The catalyst is removed from the reaction mixture by filtration through a Celite pad and the filtrate is concentrated in vacuo. The residue obtained is triturated in acetonitrile, and filtered to provide 6-Amino-7-methyl-1H-benzimidazole-4-carbonitrile (10), as a tan solid (0.768 g, 90% Yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07304084B2
Source datasetuspto-grants-2007_12
ORD IDord-58f400fa5f094b26ab26f318e775f936
Source noteuspto-grants-2007_12