HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → (1-Methylethyl) [3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]phenyl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 4-Methoxy-6-methylpyrimidin-2-amine | HCID 587236 | — |
| Reactant | m-Isocyanatobenzenesulfonyl isocyanate | HCID 13138205 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (1-Methylethyl) [3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]phenyl]carbamate | HCID 13138206 | — |
Reaction Steps
To an anhydrous solutiion o 2.3 g of m-isocyanatobenzenesulfonyl isocyanate in 50 ml of methylene chloride was added in small portions 1.4 g of 2-amino-4-methoxy-6-methylpyrimidine. Efficient stirring was maintained during the addition and for three additional hours. The intermediate thus obtained, 3-isocyanato-N-[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]benenesulfonamide, was reacted further by adding one gram of 2-propanol and stirring the resultant mixture for an additional sixteen hours. Filtration of the reaction mixture and evaporation of the filtrate yielded the desired product melting at 173°-180°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04225337 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-117ab8697f8f439cae2eb0a9f17a5622 |
| Source note | uspto-grants-1980_09 |