HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → 6-chloro-N-(3-methylsulphonylaminobenzyl)nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 6-Bromonicotinic acid | HCID 238932 | — |
| Reactant | N-[3-(Aminomethyl)phenyl]methanesulfonamide | HCID 10495443 | — |
| Product | 6-chloro-N-(3-methylsulphonylaminobenzyl)nicotinamide | HCID 21914545 | — |
Reaction Steps
6-Bromonicotinic acid (200 mg, 0.99 mmol) was heated at reflux in thionyl chloride (2 ml) for 3 hrs. The reaction was allowed to cool to room temperature and the excess thionyl chloride evaporated under vacuum. The residue was dissolved in DCM (2 ml), 3-methylsulphonylaminobenzylamine (200 mg, 0.10 mmol) and sodium carbonate (500 mg) were added to the solution. The reaction was stirred at room temperature for 4 hrs, filtered and the filtrate reduced to dryness under vacuum to give 6-chloro-N-(3-methylsulphonylaminobenzyl)nicotinamide. NMR: δH [2H6]-DMSO 9.30,(1H, t), 8.88,(1H, d), 8.28,(1H, dd), 7.67,(1H, d), 7.23,(1H, t), 7.10,(1H, s), 7.04,91H, d), 6.97,(1H, d), 4.45,(2H, d), 2.90,(3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07125898B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-57914acc94d846b9a3f59b9d5a1c371a |
| Source note | uspto-grants-2006_10 |