HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Sulfide → N-[(alpha-thiocarbamoyl)furfuryl]-3-methylisothiazole-5-carboxylic acid amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(alpha-cyanofurfuryl)-3-methylisothiazole-5-carboxylic acid amide | HCID 14624283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[(alpha-thiocarbamoyl)furfuryl]-3-methylisothiazole-5-carboxylic acid amide | HCID 15080081 | — |
Reaction Steps
1.0 g of N-(alpha-cyanofurfuryl)-3-methylisothiazole- 5-carboxylic acid amide was dissolved in 30 ml of tetrahydrofuran, and 0.6 ml of triethylamine was added. With stirring at room temperature, hydrogen sulfide gas was introduced into the mixture. Five hours later, the reaction solvent was evaporated under reduced pressure. Water was added to the residue. The precipitated crystals were separated by filtration to give 1.1 g of the desired N[-(alpha-thiocarbamoyl)furfuryl]-3-methylisothiazole-5-carboxylic acid amide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04980363 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-e4c7a4f7ea3d4b30841898f512ca6111 |
| Source note | uspto-grants-1990_12 |