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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597447Generated: November 1, 2026

3-Carbamoyl-5-methylisoxazole → 5-Methylisoxazole-3-carbothioamide

https://huagongshe.com/reaction/1597447

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Carbamoyl-5-methylisoxazoleHCID 76981—
ReactantLawesson's reagentHCID 87949—
SolventTolueneHCID 1140—
Product5-Methylisoxazole-3-carbothioamideHCID 2799530103.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06294580B1
Source datasetuspto-grants-2001_09
ORD IDord-20857f6974b045459e7c3f289a5bb704
Source noteuspto-grants-2001_09