HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Thiophenecarboxylic acid, 3-(isocyanatosulfonyl)-, methyl ester → Methyl 3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-thiophenecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Thiophenecarboxylic acid, 3-(isocyanatosulfonyl)-, methyl ester | HCID 157296 | — |
| Reactant | 4-Methoxy-6-methylpyrimidin-2-amine | HCID 587236 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-thiophenecarboxylate | HCID 13390184 | — |
Reaction Steps
To 1.4 g of 2-amino-4-methoxy-6-methylpyrimidine in 30 ml of anhydrous acetonitrile was added at ambient temperature, with stirring 3.6 g of 2-methoxycarbonyl-3-thiophenesulfonylisocyanate. The mixture was heated to the boiling point and then allowed to cool to ambient temperature. After stirring for sixteen hours the precipitate present in the mixture was filtered off and washed with anhydrous ethyl ether. The product thus obtained which melted at 165°-173° showed absorption peaks by infrared spectroscopy at 1720 and 1700 cm-1, consistent for the carbonyl groups in the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04701535 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-71fdcd695fb245e8be245884ebf3a9da |
| Source note | uspto-grants-1987_10 |