HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-(thiazolo[4,5-c]pyridin-2-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | (1,3)Thiazolo(4,5-c)pyridin-2-amine | HCID 14252938 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(thiazolo[4,5-c]pyridin-2-yl)acetamide | HCID 15593545 | 46% |
Reaction Steps
To a suspension of 2-aminothiazolo[4,5-c]pyridine [prepared according to the procedure in T. Takahashi et al., Pharm. Bull. (Japan) 2, 34 (1954)] (151 mg, 1 mmole) in acetic anhydride (1 ml) was added pyridine (1 ml), and the mixture was heated at 100°-120° C. for an hour. After cooling, the mixture was diluted with CH2Cl2 (20 ml). The resulting precipitate was collected by filtration and recrystallized from methanol (20 ml) to give 90 mg of the title compound as fine needles (46%). Mp. >212° C. (sub.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04500526 |
| Source dataset | uspto-grants-1985_02 |
| ORD ID | ord-6bf54af24dff478f8ba524d9b280aff5 |
| Source note | uspto-grants-1985_02 |