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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164734Generated: November 2, 2026

2-Amino-4,6-dimethyl-3-pyridinecarbonitrile → N-[(3-Cyano-4,6-dimethylpyridin-2-yl)aminocarbonyl]-2-nitrobenzenesulfonamide

https://huagongshe.com/reaction/1164734

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4,6-dimethyl-3-pyridinecarbonitrileHCID 230471—
Reactant2-Nitrobenzenesulfonyl isocyanateHCID 11138884—
SolventAcetonitrileHCID 6342—
ProductN-[(3-Cyano-4,6-dimethylpyridin-2-yl)aminocarbonyl]-2-nitrobenzenesulfonamideHCID 14050202—

Reaction Steps

To a stirred suspension of 0.5 g (3.4 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, 1H), 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04906288
Source datasetuspto-grants-1990_03
ORD IDord-a2f2a3e8b51742c58bd0747ae1ed8a1e
Source noteuspto-grants-1990_03