Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855354Generated: October 26, 2026

1H-Indole-7-carboxylic acid → HCID 86603058, compound

https://huagongshe.com/reaction/855354

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-butylbenzyl)-[2-(4-chlorophenyl)-ethyl]-amineHCID 29792506—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86603058HCID 8660305895.9%

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, 91 mg (0.3 mmol) (4-tert-butyl-benzyl)-[2-(4-chloro-phenyl)-ethyl]-amine in 1 ml DMF was added. After stirring for 3 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 yellow solid foam was purified by column chromatography (8 g silica gel; heptane/EtOAc 9:1) to give 128 mg (86%) of a 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-bf4a111da22b4f0fb9d44fcfc7b2d543
Source noteuspto-grants-2007_08