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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216635Generated: October 25, 2026

Water → 2-Aminocarbonylamino-6-(1-hydroxyethyl)indole-3-carboxamide

https://huagongshe.com/reaction/216635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant6-Acetyl-2-aminocarbonylaminoindole-3-carboxamideHCID 59189775—
SolventTetrahydrofuranHCID 8028—
Product2-Aminocarbonylamino-6-(1-hydroxyethyl)indole-3-carboxamideHCID 5918988622%

Reaction Steps

Sodium borohydride (10 mg, 0.26 mmol) was added to a solution of 6-acetyl-2-aminocarbonylaminoindole-3-carboxamide (Compound 14-1,14 mg, 0.054 mmol) in anhydrous tetrahydrofuran (2 mL) under ice-cooling, and the mixture was stirred at room temperature for 1 hour. Water (5 mL) was added to the reaction mixture, and the whole was extracted with ethyl acetate (20 mL). The organic layer was washed with brine (5 mL), and dried over anhydrous magnesium sulfate. After the solvent was evaporated under reduced pressure, the resultant solid was washed with diethyl ether (2 mL) and dried under reduced pressure to give the title compound (3 mg) as a colorless solid (yield 22%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193237B2
Source datasetuspto-grants-2012_06
ORD IDord-c3ede20c1faf4393a8be07f577c14b7f
Source noteuspto-grants-2012_06