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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012055Generated: October 26, 2026

1,2-Dichloroethane → cyclohexanecarboxylic acid [3-(1H-benzimidazol-2-yl)-1H-pyrazol-4-yl]-amide

https://huagongshe.com/reaction/1012055

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantCyclohexanecarboxylic acidHCID 7413—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 178508052HCID 178508052—
SolventDimethyl SulfoxideHCID 679—
Productcyclohexanecarboxylic acid [3-(1H-benzimidazol-2-yl)-1H-pyrazol-4-yl]-amideHCID 17852241832.3%

Reaction Steps

A mixture of cyclohexanecarboxylic acid (36 mg, 0.28 mmol), 3-(1H-benzimidazol-2-yl)-1H-pyrazol-4-ylamine (50 mg, 0.25 mmol), EDC (58 mg, 0.30 mmol) and HOBt (41 mg, 0.30 mmol) in DMSO (2 ml) was stirred at ambient temperature for 24 h. The reaction mixture was partitioned between EtOAc (40 ml) and water (40 ml) and the organic portion dried (MgSO4), filtered and reduced in vacuo. The residue was purified by flash column chromatography [SiO2, EtOAc-petrol (1:4, 1:3, 1:2, 1:1)] affording cyclohexanecarboxylic acid [3-(1H-benzimidazol-2-yl)-1H-pyrazol-4-yl]-amide as an off-white solid (25 mg, 32%). (LC/MS: Rt 3.59, [M+H]+ 310.16).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977477B2
Source datasetuspto-grants-2011_07
ORD IDord-0080935165ce4572b099b98f55830e10
Source noteuspto-grants-2011_07