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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097227Generated: October 25, 2026

Water → 3-Amino-4,5,6,7-tetrahydrobenzo[1,2-b]selenophene-2-carboxamide

https://huagongshe.com/reaction/1097227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant3-Amino-4,5,6,7-tetrahydrobenzo[1,2-b]selenophene-2-carbonitrileHCID 59547212—
SolventEthanolHCID 702—
Product3-Amino-4,5,6,7-tetrahydrobenzo[1,2-b]selenophene-2-carboxamideHCID 5954722354%

Reaction Steps

To a suspension of 3-amino-4,5,6,7-tetrahydrobenzo[1,2-b]selenophene-2-carbonitrile (2.4 g) in ethanol (50 mL) was added aqueous sodium hydroxide solution (50 mL, 10%) at rt and the mixture was refluxed for 1 h. The cooled reaction mixture was poured into ice cooled water and stirred for 15 min. The precipitated solid filtered, washed with cold water and dried to give the product as a pale brown color solid (1.4 g, 54%), mp 152-154° C. 1H NMR (400 MHz, DMSO-d6): δ 6.58 (1H, s, —CONH2), 6.45 (1H, s, —CONH2), 2.66 (2H, s, H-7), 2.24 (2H, s, H-4), 1.73 (4H, s, H-5,6); LC-MS (positive ion mode): m/z 265, 267 (M+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143237B2
Source datasetuspto-grants-2012_03
ORD IDord-3f6a2192ebba4248a07578a987bf48c3
Source noteuspto-grants-2012_03