Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855341Generated: October 28, 2026

1H-Indole-7-carboxylic acid → HCID 86603046, compound

https://huagongshe.com/reaction/855341

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Indole-7-carboxylic acidHCID 74281—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 69343188HCID 69343188—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86603046HCID 8660304655.2%

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, 69 mg (0.3 mmol) of (4-tert-butyl-benzyl)-pent-4-enyl-amine in 1 ml DMF was 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 resulting oil was purified by column chromatography (8 g silica gel; heptane/EtOAc 6:1) to give 62 mg (53%) of a light yellow viscous oil. MS (ISP) 375.5 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-b451d1b1760b4c8396132536b11f7852
Source noteuspto-grants-2007_08