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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380382Generated: November 1, 2026

2-Chlorobenzimidazole → HCID 86585568, compound

https://huagongshe.com/reaction/380382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzimidazoleHCID 78572—
ReactantHCID 18677412HCID 18677412—
CatalystCopperHCID 23978—
SolventChloroformHCID 6212—
ProductHCID 86585568HCID 8658556833.9%

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 2-chloro-1H-benzimidazole (0.015 mol), intermediate 16 (0.015 mol) and copper (0.015 mol) was stirred in an oil bath at 180° C. The mixture was cooled and the product was dissolved in CHCl3 (50 ml). The solution was filtered over dicalite and the filtrate was evaporated. The residue was purified by column chromatography over silica gel (eluent: CHCl3/(CH3OH/NH3) 95/5). The pure fractions were collected and the solvent was evaporated. The residue was dissolved in CH3CN (50 ml) and converted into the hydrochloric acid salt (1:2) with HCl/2-propanol. The salt was filtered off, washed on filter with cold CH3CN (20 ml), then dried, yielding 1.1 g (17%) of N-1H-benzimidazol-2-yl-1,3,4,5-tetrahydro-5-methyl-2H-pyrido [4,3-b]indole-2-propanamine dihydrochloride.hemihydrate (compound 105).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06303614B1
Source datasetuspto-grants-2001_10
ORD IDord-f506014a3c694c8da424af66248dc33d
Source noteuspto-grants-2001_10