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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098244Generated: November 1, 2026

HCID 67387379, compound → HCID 67387004, compound

https://huagongshe.com/reaction/2098244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67387379HCID 67387379—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 67387004HCID 6738700469.4%

Reaction Steps

3-Nitro-3′-trifluoromethoxy-biphenyl-4-ylamine (28.5 g) was dissolved in methanol (250 mL). To this solution, Pd—C (10%, Degussa Type, 15 g) was added, and the resulting mixture was stirred under a hydrogen atmosphere for 4 hours. The solution was filtered on celite, washed with methanol, and then concentrated to give 3′-trifluoromethoxy-biphenyl-3,4-diamine (17.8 g) which was used without further purification. 3′-Trifluoromethoxy-biphenyl-3,4-diamine (17.8 g) was taken up into methanol (100 mL), and cyanogen bromide (8.9 g) was added. The resulting mixture was stirred at room temperature for about 30 minutes. The solution was concentrated to dryness. The resulting crude product was triturated with diethyl ether (100 mL), filtered and dried to obtain 5-(3-trifluoromethoxy-phenyl)-1H-benzoimidazol-2-ylamine hydrobromide salt (21.3 g), which was used without further purification. LCMS (m/z): 293.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450354B2
Source datasetuspto-grants-2013_05
ORD IDord-b7046d0de7a24b09a59e472bfe7b4787
Source noteuspto-grants-2013_05