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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855383Generated: October 26, 2026

1H-Indole-7-carboxylic acid → [Rac]-1h-indole-7-carboxylic acid (4-tert-butyl-benzyl)-[2-(4-fluoro-phenyl)-2-hydroxy-ethyl]-amide

https://huagongshe.com/reaction/855383

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Indole-7-carboxylic acidHCID 74281—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant[Rac]-(4-tert-butyl-benzyl)-[2-(4-fluoro-phenyl)-2-hydroxy-ethyl]-amineHCID 69342608—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product[Rac]-1h-indole-7-carboxylic acid (4-tert-butyl-benzyl)-[2-(4-fluoro-phenyl)-2-hydroxy-ethyl]-amideHCID 6951342167.5%

Reaction Steps

To a solution of 80 mg (0.5 mmol) of 1H-indole-7-carboxylic acid and 159 mg of TBTU (0.5 mmol) in 6 ml DMF, were added 0.43 ml (2.48 mmol) of N,N-diisopropylethyl amine. After stirring for 5 min at rt, 150 mg (0.5 mmol) of [rac]-(4-tert-butyl-benzyl)-[2-(4-fluoro-phenyl)-2-hydroxy-ethyl]-amine were added. After stirring for 17 h at rt, the reaction mixture was diluted with 60 ml water and extracted with EtOAc (2×). 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 (40 g silica gel; heptane/EtOAc 2:1) to give 150 mg (66%) of an white solid. MS (ISP) 445.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-50fa719f04ca4a9bb2777f72ff1376cf
Source noteuspto-grants-2007_08