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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855409Generated: October 26, 2026

Diisopropylethylamine → 5-Chloro-1H-indole-7-carboxylic acid (4-tert-butyl-benzyl)-[2-(3-difluoromethoxy-phenyl)-ethyl]-amide

https://huagongshe.com/reaction/855409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant5-chloro-1H-indole-7-carboxylic acidHCID 66868563—
ReactantHCID 68576819HCID 68576819—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-Chloro-1H-indole-7-carboxylic acid (4-tert-butyl-benzyl)-[2-(3-difluoromethoxy-phenyl)-ethyl]-amideHCID 8660309974.4%

Reaction Steps

To a solution of 59 mg (0.3 mmol) of 5-chloro-1H-indole-7-carboxylic acid and 96 mg of TBTU (0.3 mmol) in 3 ml DMF, were added 0.26 ml (1.5 mmol) of N,N-diisopropylethyl amine. After stirring for 5 min at rt, 100 mg (0.3 mmol) of (4-tert-butyl-benzyl)-[2-(3-difluoromethoxy-phenyl)-ethyl]-amine in 2 ml DMF were added. After stirring for 4 h at rt, the reaction mixture was diluted with 50 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 (8 g silica gel; EtOAc/heptane 1:6) to give 114 mg white solid (67%). MS(ISP) 512.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-2699d8674a6048c19a4cee915c4765ed
Source noteuspto-grants-2007_08