HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463975Generated: October 27, 2026
Benzoic acid, 2-(isocyanatosulfonyl)-, methyl ester → Methyl 2-[(4-methoxy-6-methyl-pyrimidin-2-yl)carbamoylsulfamoyl]benzoate
https://huagongshe.com/reaction/463975
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoic acid, 2-(isocyanatosulfonyl)-, methyl ester | HCID 156281 | — |
| Reactant | 4-Methoxy-6-methylpyrimidin-2-amine | HCID 587236 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-[(4-methoxy-6-methyl-pyrimidin-2-yl)carbamoylsulfamoyl]benzoate | HCID 13176578 | 21.1% |
Reaction Steps
To a stirred suspension of 1.4 g of 2-amino-4-methoxy-6-methylpyrimidine in 30 ml of anhydrous methylene chloride was added at ambient temperature 2.4 g of 2-methoxycarbonylbenzenesulfonylisocyanate. After stirring for 16 hours, the foregoing mixture was filtered to remove unreacted amine, and the filtrate evaporated at temperatures up to 40° and reduced pressure. The resultant residue was stirred in 25 ml of water, the pH adjusted to 10 by the addition of 50% sodium hydroxide and the solution filtered. Acidification of the filtrate to pH 3 with hydrochloric acid caused precipitation of the desired product which was removed by filtration and dried to yield 0.8 g of product melting at 173°-179°. It showed infrared absorption peaks at 1720, 1680, 1630 and 1550 cm-1, consistent for N-[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-2-methoxycarbonylbenzenesulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04545808 |
|---|
| Source dataset | uspto-grants-1985_10 |
|---|
| ORD ID | ord-e31e84383a91465b8e71ed659ea11ff6 |
|---|
| Source note | uspto-grants-1985_10 |
|---|