HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 17416722, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-{[5-(2-amino-1,3-thiazol-4-yl)thiophen-2-yl]methyl}acetamide | HCID 2560398 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 17416722 | HCID 17416722 | — |
Reaction Steps
To a suspension of 5.0 g of 2-amino-4-(5-acetylaminomethyl-2-thienyl]thiazole in 200 ml of chloroform is added 12 ml of triethylamine, and is added dropwise 1.7 g of acetyl chloride with stirring at room temperature. The whole mixture is stirred at room temperature for an hour. After completion of the reaction, the resultant mixture is washed with water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. After the residue is crystallized from ethanol, the crystals are collected by filtration and recrystallized from ethanol to give 2-acetylamino-4-(5-acetylaminomethyl-2-thienyl)thiazole, melting at 251° C. with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04720493 |
| Source dataset | uspto-grants-1988_01 |
| ORD ID | ord-b941a805f8594bfd83231ce775ea1824 |
| Source note | uspto-grants-1988_01 |