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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505765Generated: October 31, 2026

1-Hydroxybenzotriazole → N-[2-(Trifluoromethyl)benzyl]-5-({[2-(trifluoromethyl)phenyl]carbonyl}amino)-2,3-dihydro-1-benzofuran-7-carboxamide

https://huagongshe.com/reaction/1505765

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant2-(Trifluoromethyl)benzylamineHCID 76447—
ReactantHCID 90229275HCID 90229275—
ReactantHCID 178458058HCID 178458058—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductN-[2-(Trifluoromethyl)benzyl]-5-({[2-(trifluoromethyl)phenyl]carbonyl}amino)-2,3-dihydro-1-benzofuran-7-carboxamideHCID 71532088—

Reaction Steps

To a solution of 5-({[2-(trifluoromethyl)phenyl]carbonyl}amino)-2,3-dihydro-1-benzofuran-7-carboxylic acid (35 mg) in DMF (2 mL), N′-(ethylcarbonimidoyl)-N,N-dimethyl-1,3-propanediamine hydrochloride (23 mg), 1-hydroxybenzotriazol (23 mg) and triethylamine (17 μL) were added. Under ice-cooling, to the mixture was added 2-(trifluoromethyl)benzylamine (15 μL), and it was stirred at room temperature overnight. The reaction mixture was poured into ice water, and extracted with ethyl acetate. The ethyl acetate layer was washed sequentially with water and brine, dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was washed with n-hexane/ethyl acetate (1:1) and collected by filtration to obtain the titled compound (43 mg) as colorless powder. MS (ESI+) m/z 509 (M+H)+, Rt=2.31 minutes (method A)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216968B2
Source datasetuspto-grants-2015_12
ORD IDord-e8ff3c10c01d4f92bd89a9a451a210e2
Source noteuspto-grants-2015_12