HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → C-(4-methanesulfonyl-phenyl)-N-thiazol-2-yl-methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | 4-(Methylsulfonyl)benzenemethanesulfonyl chloride | HCID 21962418 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | C-(4-methanesulfonyl-phenyl)-N-thiazol-2-yl-methanesulfonamide | HCID 86602239 | — |
Reaction Steps
To the solution of the title B compound, (4-methanesulfonyl-phenyl)-methanesulfonyl chloride (1.86 mmol, 0.5 g) in 5 mL of pyridine is added 2-aminothiazole (2.5 mmol, 0.25 g) and the mixture is stirred for 48 h. The reaction mixture is quenched with aqueous 1 N HCl and the product is taken up in EtOAc, dried and concentrated to afford C-(4-methanesulfonyl-phenyl)-N-thiazol-2-yl-methanesulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07812167B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-e647cf369cb744ceabbcc9d074c9dcf1 |
| Source note | uspto-grants-2010_10 |