Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855371Generated: October 26, 2026

Diisopropylethylamine → HCID 86603075, compound

https://huagongshe.com/reaction/855371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant(4-Tert-butylbenzyl)-[2-(4-chlorophenyl)-ethyl]-amineHCID 29792506—
Reactant5-chloro-1H-indole-7-carboxylic acidHCID 66868563—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86603075HCID 8660307545.2%

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, 91 mg (0.3 mmol) of (4-tert-butyl-benzyl)-[2-(4-chloro-phenyl)-ethyl]-amine in 2 ml DMF were added. After stirring for 2 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 65 mg white solid (42%). MS (ISP) 479.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-cbdfa63a9df74b1691ae1b2723458f4b
Source noteuspto-grants-2007_08