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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788607Generated: October 29, 2026

Hydrochloric Acid → 2-[2-[5-Chloro-2-(4-chlorophenyl)phenyl]-6-quinolyl]-1-cyclohexyl-benzimidazole-5-carboxylic acid

https://huagongshe.com/reaction/1788607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactant1-(4'-Chloro-4-chloro-biphen-2-yl)-ethanoneHCID 54395380—
Reactant2-(4-amino-3-formyl-phenyl)-1-cyclohexyl-1H-benzoimidazole-5-carboxylic acid ethyl esterHCID 86600382—
SolventEthanolHCID 702—
Product2-[2-[5-Chloro-2-(4-chlorophenyl)phenyl]-6-quinolyl]-1-cyclohexyl-benzimidazole-5-carboxylic acidHCID 527615289.1%

Reaction Conditions

Temperature75 °C

Reaction Steps

1-(4′-Chloro-4-chloro-biphen-2-yl)-ethanone (132 mg, 0.5 mmol) and 2-(4-amino-3-formyl-phenyl)-1-cyclohexyl-1H-benzoimidazole-5-carboxylic acid ethyl ester (98 mg, 0.25 mmol) were dissolved in 500 μL ethanol and 500 μL 10% ethanolic KOH were added. The reaction was stirred at 75° C. overnight. The reaction was acidified with 4N hydrochloric acid, extracted three times with ethyl acetate, the organic extracts were dried with sodium sulfate and then evaporated. Purification via reverse-phase HPLC gave 132 mg product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511145B2
Source datasetuspto-grants-2009_03
ORD IDord-d05b9a35d6b640619d0c5b71820127fe
Source noteuspto-grants-2009_03