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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628392Generated: November 2, 2026

2,4-Dichloroaniline → Ethyl [4-chloro-2-[(2,4-dichlorophenyl)amino]-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]acetate

https://huagongshe.com/reaction/1628392

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichloroanilineHCID 11123—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl [2,4-dichloro-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]acetateHCID 86632860—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductEthyl [4-chloro-2-[(2,4-dichlorophenyl)amino]-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]acetateHCID 8663286112%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of ethyl [2,4-dichloro-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]acetate (708 mg, 2.06 mmol), 2,4-dichloroaniline (1.00 g, 6.19 mmol) and N-methyl-2-pyrrolidinone (0.5 mL) was stirred at 100° C. for 3.5 days. After cooling, the reaction mixture was neutralized with saturated aqueous sodium hydrogen carbonate and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by basic silica gel column chromatography eluting with a 3-15% ethyl acetate/n-hexane gradient mixture. The resulting solid was washed with n-hexane to give the title compound (115 mg, 0.245 mmol, 12%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785460B2
Source datasetuspto-grants-2014_07
ORD IDord-e3338e2d75a946df8a0703ab8302e290
Source noteuspto-grants-2014_07