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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,6-Dichloro-4-(trifluoromethyl)phenylacetic acid | HCID 2736872 | — |
| Reactant | N2-Methylbenzene-1,2,3-triamine | HCID 12296380 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-[2,6-Dichloro-4-(trifluoromethyl)benzyl]-1-methyl-1H-benzimidazol-7-amine | HCID 59202090 | 45.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039500B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-2bee90d555524516ab1e2fed9718c21c |
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| Source note | uspto-grants-2011_10 |
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