HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 20154303, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acetoxyacetyl chloride | HCID 26297 | — |
| Reactant | HCID 20154278 | HCID 20154278 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 20154303 | HCID 20154303 | — |
Reaction Steps
To a suspension of 2-amino-4-(5-aminomethyl-2-thienyl) thiazole in 150 ml of chloroform is added 10 ml of triethylamine, and 3.1 g of acetoxyacetylchloride is added dropwise with stirring at room temperature (10°-35° C.). The whole mixture is stirred at room temperature for an hour, and then washed with water. The organic layer is separated, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue is recrystallized from ethanol to give 2-amino-4-(5-acetoxyacetylaminomethyl-2-thienyl) thiazole, melting at 149°-150° C. The corresponding maleate melts at 153°-154° C. with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04720493 |
| Source dataset | uspto-grants-1988_01 |
| ORD ID | ord-69ef727b6cb54d4abd86a08b82df35de |
| Source note | uspto-grants-1988_01 |