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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855362Generated: October 28, 2026

1H-Indole-7-carboxylic acid → 1H-Indole-7-carboxylic acid (4-tert-butyl-benzyl)-[2-(4-trifluoromethyl-phenyl)-ethyl]-amide

https://huagongshe.com/reaction/855362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Indole-7-carboxylic acidHCID 74281—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant(4-Tert-butyl-benzyl)-[2-(4-trifluoromethyl-phenyl)-ethyl]-amineHCID 69342584—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1H-Indole-7-carboxylic acid (4-tert-butyl-benzyl)-[2-(4-trifluoromethyl-phenyl)-ethyl]-amideHCID 8660306676.6%

Reaction Steps

To a solution of 48 mg (0.3 mmol) of 1H-indole-7-carboxylic acid and 96 mg of TBTU (0.3 mmol) in 4 ml DMF, were added 0.26 ml (1.5 mmol) of N,N-diisopropylethyl amine. After stirring for 5 min at rt, 101 mg (0.3 mmol) (4-tert-butyl-benzyl)-[2-(4-trifluoromethyl-phenyl)-ethyl]-amine in 1 ml DMF was added. After stirring for 17 h at rt, the reaction mixture was diluted with 50 ml water and extracted with 2×50 ml EtOAc. The combined organic phases were washed with water and brine, dried with magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography (8 g silica gel; EtOAc/heptane 1:9) to give 110 mg colorless viscous oil (71%). MS (ISP) 479.5 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-13b657b3cf5b4a4ba21a500daffc02d1
Source noteuspto-grants-2007_08