HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Acetyl-2-amino-4-methylthiazole → N-(5-acetyl-4-methyl-1,3-thiazol-2-yl)-4-propylbenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Acetyl-2-amino-4-methylthiazole | HCID 720882 | — |
| Reactant | 4-N-Propylbenzenesulphonyl chloride | HCID 2737222 | — |
| Product | N-(5-acetyl-4-methyl-1,3-thiazol-2-yl)-4-propylbenzenesulfonamide | HCID 11209950 | — |
Reaction Steps
The title compound was prepared from 5-acetyl-2-amino-4-methylthiazole and 4-n-propylbenzenesulfonyl chloride as described in the synthetic METHOD B to give a white solid (11.6 mg) with purity >90%: MS (pos) m/z 339.2; HEMS m/z 338.0748 (calc. of monoisotopic mass for C15H18N2O3S2 gives 338.0759).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07125900B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-ffd26df12b0e45868fb94858c4f84bf9 |
| Source note | uspto-grants-2006_10 |