Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788606Generated: November 3, 2026

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

https://huagongshe.com/reaction/1788606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactant1-(4'-Chloro-4-nitro-biphen-2-yl)-ethanoneHCID 86027063—
Reactant2-(4-amino-3-formyl-phenyl)-1-cyclohexyl-1H-benzoimidazole-5-carboxylic acid ethyl esterHCID 86600382—
SolventEthanolHCID 702—
Product2-[2-[5-Amino-2-(4-chlorophenyl)phenyl]-6-quinolyl]-1-cyclohexyl-benzimidazole-5-carboxylic acidHCID 527615412.6%

Reaction Conditions

Temperature75 °C

Reaction Steps

1-(4′-Chloro-4-nitro-biphen-2-yl)-ethanone (69 mg, 0.25 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. for 3 days. 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 18 mg product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511145B2
Source datasetuspto-grants-2009_03
ORD IDord-31f9c0f61d9249b9b6c327d0605ace27
Source noteuspto-grants-2009_03