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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628394Generated: November 1, 2026

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

https://huagongshe.com/reaction/1628394

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichloroanilineHCID 11123—
ReactantSodium BicarbonateHCID 516892—
ReactantIsopropyl [2,4-dichloro-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]acetateHCID 86632857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductIsopropyl {4-chloro-2-[(2,4-dichlorophenyl)amino]-7-(1-ethylpropyl)-1H-benzimidazol-1-yl}acetateHCID 8663286221%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of isopropyl [2,4-dichloro-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]acetate (Reference Example 10; 1.96 g, 5.49 mmol), 2,4-dichloroaniline (2.67 g, 16.5 mmol) and N-methyl-2-pyrrolidinone (1.5 mL) was stirred at 100° C. for 15 hr. After cooling, the reaction mixture was neutralized with saturated aqueous sodium hydrogen carbonate and extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting with a 3-15% ethyl acetate/n-hexane gradient mixture to give the title compound (546 mg, 1.13 mmol, 21%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785460B2
Source datasetuspto-grants-2014_07
ORD IDord-bc1f7f3ea7a54943a396a513c19472c6
Source noteuspto-grants-2014_07