HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2-Formylamino-4-chloromethylthiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Thiazolamine, 4-(chloromethyl)-, hydrochloride (1:1) | HCID 73228 | — |
| Reactant | Acetic-formic anhydride | HCID 75269 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Formylamino-4-chloromethylthiazole | HCID 10374969 | — |
Reaction Steps
To a mixture of 2-amino-4-chloromethylthiazole hydrochloride (2 g), anhydrous pyridine (3.2 g) and anhydrous N,N-dimethylformamide (10 ml) was slowly added acetic formic anhydride (1.7 g) with stirring at 0° to 5° C. After one hour of stirring, the reaction mixture was poured into cold water and extracted with ethyl acetate. The extract was washed with 1N hydrochloric acid and aqueous sodium chloride solution successively and dried over magnesium sulfate. The solvent was then distilled off and the residue was collected and dried to give 2-formylamino-4-chloromethylthiazole (0.94 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04742057 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-3433127cf1e74b63be700ee89918855c |
| Source note | uspto-grants-1988_05 |