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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111407Generated: October 29, 2026

Hydrogen Sulfide → N-[(alpha-thiocarbamoyl)furfuryl]-3-methylisothiazole-5-carboxylic acid amide

https://huagongshe.com/reaction/1111407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen SulfideHCID 402—
ReactantTriethylamineHCID 8471—
ReactantN-(alpha-cyanofurfuryl)-3-methylisothiazole-5-carboxylic acid amideHCID 14624283—
SolventTetrahydrofuranHCID 8028—
ProductN-[(alpha-thiocarbamoyl)furfuryl]-3-methylisothiazole-5-carboxylic acid amideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04980363
Source datasetuspto-grants-1990_12
ORD IDord-e4c7a4f7ea3d4b30841898f512ca6111
Source noteuspto-grants-1990_12