HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Sulfide → 2-Cyclopropylamino-4-methyl-thiazole-5-carboxylic acid (thiocarbamoyl-thiophen-2-yl-methyl)-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Cyclopropylamino-4-methyl-thiazole-5-carboxylic acid (cyano-thiophen-2-yl-methyl)-amide | HCID 54367202 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Cyclopropylamino-4-methyl-thiazole-5-carboxylic acid (thiocarbamoyl-thiophen-2-yl-methyl)-amide | HCID 54329897 | 88% |
Reaction Steps
0.72g of 2-cyclopropylamino-4-methyl-thiazole-5-carboxylic acid (cyano-thiophen-2-yl-methyl)-amide (12) was dissolved in 10ml of ethanol and then 0.63ml of triethylamine was added thereto. The reaction solution was stirred under reflux for 8 hours while introducing hydrogen sulfide gas. After removing the solvent, water was added to the residue and then the solid product which is not dissolved in water was filtered. The filtered solid product was washed with diethylether and then dried to obtain 0.70g (Yield 88%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05514643 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-e50cfb74c4cd4ca6b45e05c723e1a1f7 |
| Source note | uspto-grants-1996_05 |