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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62645Generated: October 26, 2026

Water → 1H-Indole-2-carboxamide

https://huagongshe.com/reaction/62645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIndole-2-carboxylic acidHCID 72899—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDimethylformamideHCID 6228—
Product1H-Indole-2-carboxamideHCID 594832—

Reaction Steps

To a solution of substituted indole-2-carboxylic acid (1e: 1 mmol) in dry DMF (4 mL) were added HATU (1.5 eq.) and the desired amine (R6—NH2: 1.2 eq.) followed by DIPEA (5.0 eq.) at 0° C. The resulting mixture was stirred at room temperature for 12 h to 24 h. To the reaction mixture water (10 mL) was added and stirred for 10 minutes. The resultant solid was collected by filtration, washed with water, hexane and dried. In some instances reaction mixture was extracted with ethyl acetate. The organic layer was washed with water, brine, dried over anhydrous Na2SO4 and concentrated under reduced pressure. The crude compounds were purified by column chromatography over silica gel (100-200 mesh) or CombiFlash® purification system (Teledyne Isco) using appropriate mixtures of ethyl acetate and hexanes/petroleum ether or preparative HPLC to obtain the desired product indole-2-carboxamide (I).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447039B2
Source datasetuspto-grants-2016_09
ORD IDord-7ef158f6c6f34d80963be8687ce81787
Source noteuspto-grants-2016_09