HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-4,6-dimethyl-3-pyridinecarbonitrile → N-[(3-Cyano-4,6-dimethylpyridin-2-yl)aminocarbonyl]-2-nitrobenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-4,6-dimethyl-3-pyridinecarbonitrile | HCID 230471 | — |
| Reactant | 2-Nitrobenzenesulfonyl isocyanate | HCID 11138884 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-[(3-Cyano-4,6-dimethylpyridin-2-yl)aminocarbonyl]-2-nitrobenzenesulfonamide | HCID 14050202 | — |
Reaction Steps
To a stirred suspension of 0.5 g (4.3 mmol) 2-amino-4,6-dimethyl-3-pyridinecarbonitrile [Archiv. Pharm., 288, 174 (1955)] in 20 ml of acetonitrile was added 1.3 g (5.7 mmol) o-nitrobenzenesulfonyl isocyanate. The mixture was then heated to reflux (80°) for four hours followed by stirring at ambient temperature overnight. A crystalline product was collected, 0.5 g, m.p. 174°-176° dec. An infrared spectrum (nujol mull) exhibited absorptions at 1700, 1720 and 2240 cm-1 ; and a proton magnetic resonance spectrum (90 MHz NMR) exhibited absorptions at 2.5 (s, 3H), 2.6 (s, 3H), 7.05 (s, H), 7.7 (s br, NH), 7.8 (m, 3H), 8.4 (m, 1H), 9.7 (s br, NH) ppm indicating the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04723991 |
| Source dataset | uspto-grants-1988_02 |
| ORD ID | ord-a4c6ac19a65248798aac4e008fbbaf15 |
| Source note | uspto-grants-1988_02 |