HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Dimethoxy-4-aminopyrimidine → N-[(2,6-dimethoxypyrimidin-4-yl)aminocarbonyl]-2-methylbenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Dimethoxy-4-aminopyrimidine | HCID 76789 | — |
| Reactant | o-Toluenesulfonyl Isocyanate | HCID 2733313 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[(2,6-dimethoxypyrimidin-4-yl)aminocarbonyl]-2-methylbenzenesulfonamide | HCID 23342477 | — |
Reaction Steps
To a stirred mixture of 2.40 g of 4-amino-2,6-dimethoxypyrimidine in 40 ml methylene chloride at ambient temperature and pressure was slowly added 3.0 g of 2-methylbenzenesulfonylisocyanate. The reaction was stirred 40 minutes, filtered, and the solid thereby obtained was washed with a small amount of acetonitrile; yield 4.0 g, m.p. 174°-175°, NMR (DMSO-d6) relative to tetramethylsilane: δ 2.77, S, area 30; δ 4.05, S, area 60; δ 6.85, S, area 89; δ 7.7-8.6, multiplets, area 45; δ 10.00, S, area 9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04221585 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-f3ed94953db04dcfa87506272299f2c5 |
| Source note | uspto-grants-1980_09 |