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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665224Generated: October 26, 2026

2,6-Dichloro-4-(trifluoromethyl)phenylacetic acid → 2-[2,6-Dichloro-4-(trifluoromethyl)benzyl]-1-methyl-1H-benzimidazol-7-amine

https://huagongshe.com/reaction/1665224

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dichloro-4-(trifluoromethyl)phenylacetic acidHCID 2736872—
ReactantN2-Methylbenzene-1,2,3-triamineHCID 12296380—
SolventTolueneHCID 1140—
Product2-[2,6-Dichloro-4-(trifluoromethyl)benzyl]-1-methyl-1H-benzimidazol-7-amineHCID 5920209045.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of [2,6-dichloro-4-(trifluoromethyl)phenyl]acetic acid (273 mg, 1.00 mmol) in toluene (2.0 mL) was added N,N′-carbonyldiimidazole (162 mg, 1.00 mmol) at room temperature. After the reaction mixture was stirred at 50° C. for 15 min, N2-methylbenzene-1,2,3-triamine (137 mg, 1.00 mmol) in toluene (2 mL) was added to the mixture, and the mixture was refluxed for further 60 hr. After the reaction mixture was cooled, the solvent was evaporated in vacuo, and the residue was purified by silica gel column chromatography eluting with 40-60% ethyl acetate/n-hexane gradient mixture to give the title compound (170 mg, 0.455 mmol, 45%) as a colorless solid. The resulting solid was recrystallized from n-hexane/ethyl acetate to give the title compound (137 mg, 0.38 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039500B2
Source datasetuspto-grants-2011_10
ORD IDord-2bee90d555524516ab1e2fed9718c21c
Source noteuspto-grants-2011_10