HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Amino-4,5,6,7-tetrahydrobenzo[1,2-b]selenophene-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Amino-4,5,6,7-tetrahydrobenzo[1,2-b]selenophene-2-carbonitrile | HCID 59547212 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Amino-4,5,6,7-tetrahydrobenzo[1,2-b]selenophene-2-carboxamide | HCID 59547223 | 54% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143237B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-3f6a2192ebba4248a07578a987bf48c3 |
| Source note | uspto-grants-2012_03 |