HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → N-[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-8-quinolinesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 8-Quinolinesulfonamide | HCID 94464 | — |
| Reactant | Methyl (4-methoxy-6-methylpyrimidin-2-yl)carbamate | HCID 13072161 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-8-quinolinesulfonamide | HCID 13072162 | 47.8% |
Reaction Steps
To a stirred mixture of 8-quinolinesulfonamide (4.2 g) in 100 ml methylene chloride is added a 2 M toluene solution of trimethylaluminum (15 ml). The resulting solution is stirred under N2 for 45 min. Solid methyl (4-methoxy-6-methylpyrimidin-2-yl)carbamate (4.0 g) is added and the mixture is heated at reflux for 60 hrs. The reaction is quenched sequentially with acetic acid (2 ml) 6 N HCl (5 ml) and water (25 ml). The organic solution is retained, dried with MgSO4, filtered, and is concentrated in vacuo to a crude solid. Washing with methyl acetate afforded 3.6 g of a pale yellow powder m.p. 181°-185° C. The infrared spectrum showed characteristic absorption bands at 3100 and 1700 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04453970 |
| Source dataset | uspto-grants-1984_06 |
| ORD ID | ord-20f12fe65a8a45b2b256904e61c463b9 |
| Source note | uspto-grants-1984_06 |