HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonamide → HCID 66634153, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 4-Bromo-1,3-thiazole-2-carboxylic acid | HCID 15122065 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66634153 | HCID 66634153 | — |
Reaction Steps
4-Bromo-1,3-thiazole-2-carboxylic acid (1.0 g, 4.8 mmol) were initially charged in tetrahydrofuran (10 ml). N,N′-Carbonyldiimidazole (1.17 g, 7.2 mmol) was added and the reaction mixture was heated under reflux for 1 h. Methanesulphonamide (0.69 g, 7.2 mmol) was added and, after 10 min, 1,8-diazabicyclo[5.4.0]undec-7-ene (1.10 g, 7.2 mmol). The reaction mixture was stirred at room temperature for 16 h and then the solvent was removed under reduced pressure. The residue was taken up in water and acidified with hydrochloric acid. The precipitated product was filtered off with suction. This gave 1.18 g (84% of theory) of 4-bromo-N-(methylsulphonyl)-1,3-thiazole-2-carboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08686004B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-0f645b2fd7de41bb8fcdc72664d68022 |
| Source note | uspto-grants-2014_04 |