HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → N-(2-Methylquinolin-6-yl)methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-Methylquinolin-6-amine | HCID 103148 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(2-Methylquinolin-6-yl)methanesulfonamide | HCID 19813426 | — |
Reaction Steps
Methanesulphonyl chloride (6.2 ml) was added dropwise to a stirred solution of 6-amino-2-methylquinoline (12.5 g) in pyridine (100 ml) cooled to 5°. Stirring was continued for 17 hours at room temperature. The pyridine was then removed by evaporation in vacuo, the residue diluted with aqueous sodium bicarbonate, and extracted three times with methylene chloride. The combined organic extracts were combined, dried (MgSO4) and evaporated in vacuo to give the title compound, yield 13.0 g, m.p. 151°-153°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05055473 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-791cb89a953e43a6977715154fc64535 |
| Source note | uspto-grants-1991_10 |