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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216630Generated: October 25, 2026

Water → 2-[(Aminocarbonyl)amino]-6-ethynylindole-3-carboxamide

https://huagongshe.com/reaction/216630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTBAF tetrahydrofuranHCID 11078149—
Reactant2-Aminocarbonylamino-6-triisopropylsilylethynylindole-3-carboxamideHCID 59189882—
SolventTetrahydrofuranHCID 8028—
Product2-[(Aminocarbonyl)amino]-6-ethynylindole-3-carboxamideHCID 2498906090.8%

Reaction Conditions

Temperature75 °C

Reaction Steps

1.0 M Tetrabutylammonium fluoride tetrahydrofuran solution (15 mL, 15 mmol) was added to a solution of 2-aminocarbonylamino-6-triisopropylsilylethynylindole-3-carboxamide (Compound 9-15, 4.0 g, 10 mmol) in anhydrous tetrahydrofuran (180 mL), and the mixture was stirred at 75° C. for 2.5 hours. Water (180 mL) was added to the reaction mixture, and the whole was extracted with ethyl acetate (180 mL). The organic layer was washed with brine (180 mL), and dried over anhydrous magnesium sulfate. After the solvent was evaporated under reduced pressure, the resultant solid was washed with a solution mixture of ethanol and chloroform (ethanol/chloroform=1/3, 55 mL) and dried under reduced pressure to give the title compound (2.2 g) as a slightly brown solid (yield 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193237B2
Source datasetuspto-grants-2012_06
ORD IDord-d66b68c6c1194befae0588c840fa9d43
Source noteuspto-grants-2012_06