HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Carbamoyl-5-methylisoxazole → 5-Methylisoxazole-3-carbothioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Carbamoyl-5-methylisoxazole | HCID 76981 | — |
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Methylisoxazole-3-carbothioamide | HCID 2799530 | 103.8% |
Reaction Steps
A suspension of 525 mg (4.16 mmol) of 5-methylisoxazole-3-carboxamide and 1.85 g (4.58 mmol, 1.1 equiv) of Lawesson's reagent in 15 mL of dry toluene was heated to reflux for 5 h, during which time the reaction mixture became a clear yellow color. The reaction mixture was cooled to RT and the solvent was removed in vacuo. Purification of the material by silica gel flash column chromatography using a gradient of hexane/EtOAc 5/1 to hexane/EtOAc 1/1 as eluent followed by trituration with acetonitrile, filtration to remove the solid Lawesson's reagent byproducts and removal of solvent afforded 614 mg of the title compound as a yellow oil: 1H NMR (CDCl3, 300 MHz) δ 8.05 (s, br, 2H), 6.52 (s, 1H), 2.46 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06294580B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-20857f6974b045459e7c3f289a5bb704 |
| Source note | uspto-grants-2001_09 |