HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-4,6-dimethoxypyrimidine → N-[(4,6-Dimethoxypyrimidin-2-yl)aminocarbonyl]-2-(dimethylaminosulfonyloxy)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-4,6-dimethoxypyrimidine | HCID 118946 | — |
| Reactant | 2-(Dimethylaminosulfonyloxy)benzenesulfonyl isocyanate | HCID 13473127 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[(4,6-Dimethoxypyrimidin-2-yl)aminocarbonyl]-2-(dimethylaminosulfonyloxy)benzenesulfonamide | HCID 13473128 | 86.7% |
Reaction Steps
To a suspension of 0.46 g (0.003 mole) 2-amino-4,6-dimethoxypyrimidine in 5 ml methylene chloride was added 1.2 g (0.004 mole) 2-(dimethylaminosulfonyloxy)-benzenesulfonyl isocyanate. The reaction exothermed (18°-26° C.) and was then stirred at room temperature 3 hours. The solvent was evaporated under reduced pressure. The resultant mixture was triturated with diethyl ether and filtered to give 1.2 g of a white solid, m.p. 165°-168° C. The infrared spectrum shows absorption bands at 1710, 1380, 1170 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04576633 |
| Source dataset | uspto-grants-1986_03 |
| ORD ID | ord-1a74b1b6e955422ea447d64bb301bce6 |
| Source note | uspto-grants-1986_03 |