HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(2-amino-2-thioxoethyl)acetamide → HCID 18956300, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(2-amino-2-thioxoethyl)acetamide | HCID 4435531 | — |
| Reactant | HCID 18956304 | HCID 18956304 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18956300 | HCID 18956300 | 49.7% |
Reaction Steps
A suspension of 2-amino-4-bromoacetylthiazole hydrobromide (14.0 g) and N-[(thiocarbamoyl)methyl]-acetamide (6.1 g) in ethanol (300 ml) was stirred at room temperature for 24 hours. The insoluble material was removed by filtration. The solvent was removed under reduced pressure. The residue was suspended in water (300 ml). The mixture was alkalized to pH 10 with a saturated aqueous potassium carbonate solution and then was extracted with a mixture of ethyl acetate (500 ml) and tetrahydrofuran (100 ml). The extract was dried over magnesium sulfate and then was evaporated to afford 4-(2-acetylaminomethylthiazol-4-yl)-2-aminothiazole (5.83 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05364871 |
| Source dataset | uspto-grants-1994_11 |
| ORD ID | ord-0577b30e88e84864981085cef14fde49 |
| Source note | uspto-grants-1994_11 |