HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminopyrimidine → Methyl 2-[[[(2-pyrimidinylamino)carbonyl]amino]sulfonyl]benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminopyrimidine | HCID 7978 | — |
| Reactant | Benzoic acid, 2-(isocyanatosulfonyl)-, methyl ester | HCID 156281 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 2-[[[(2-pyrimidinylamino)carbonyl]amino]sulfonyl]benzoate | HCID 13176579 | 65.7% |
Reaction Steps
With stirring at ambient temperature, 1.0 g of 2-aminopyrimidine in 25 ml of anhydrous acetonitrile was added to 2.4 g of 2-methoxycarbonylbenzenesulfonylisocyanate. After stirring that mixture for 24 hours, the resultant precipitate was filtered off to yield 2.2 g of the desired compound which melted at 188°-192°. Its showing infrared absorption peaks at 1700, 1680 and 1580 cm-1 is consistent for N-[(pyrimidin-2-yl)aminocarbonyl)-2-methoxycarbonylbenzenesulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04830662 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-15f7bfd5bb0e435cafe9bbf794a2eb8b |
| Source note | uspto-grants-1989_05 |