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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012060Generated: October 26, 2026

1,2-Dichloroethane → 2-[4-(2,6-difluoro-benzoylamino)-1H-pyrazol-3-yl]-1H-benzimidazole-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/1012060

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant2,3-Diaminobenzoic acid methyl esterHCID 571825—
ReactantHCID 178524951HCID 178524951—
SolventDimethylformamideHCID 6228—
Product2-[4-(2,6-difluoro-benzoylamino)-1H-pyrazol-3-yl]-1H-benzimidazole-4-carboxylic acid methyl esterHCID 17849759040.7%

Reaction Steps

A mixture of 4-(2,6-difluorobenzylamino)-1H-pyrazole-3-carboxylic acid (690 mg, 2.6 mmol) Example 16D), methyl 2,3-diaminobenzoate (415 mg, 2.6 mmol), EDC (590 mg, 3.1 mmol) and HOBt (415 mg, 3.1 mmol) in DMF (10 ml) was stirred at ambient temperature for 16 h and then reduced in vacuo. The residue was partitioned between EtOAc and brine and the organic portion dried (MgSO4), filtered, reduced then crystallised from hot EtOH. The amide intermediate (480 mg) was dissolved in AcOH (10 ml) then heated at reflux for 3 h. The reaction mixture was reduced in vacuo and then azeotroped with toluene (2×20 ml) to afford 2-[4-(2,6-difluoro-benzoylamino)-1H-pyrazol-3-yl]-1H-benzimidazole-4-carboxylic acid methyl ester (420 mg) as a fawn coloured solid. (LC/MS: Rt 3.82, [M+H]+ 398).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977477B2
Source datasetuspto-grants-2011_07
ORD IDord-e90709d967c84be6bdf1f16d4a94039b
Source noteuspto-grants-2011_07