HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Thiazolo[4,5-c]pyridine-2-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Methyl-[1,3]thiazolo[4,5-c]pyridine | HCID 640721 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Thiazolo[4,5-c]pyridine-2-carbaldehyde | HCID 15593552 | 35.5% |
Reaction Steps
A mixture of 2-methylthiazolo[4,5-c]pyridine [prepared according to the procedure of T. Takahashi et al., Pharm. Bull. (Japan) 2, 196 (1954)] (635 mg, 4.2 mmoles), 2.55 g of SeO2, 10 ml of CH3COOH and 10 ml of acetic anhydride was heated at 90 100° C. for 2.5 hours, and the reaction mixture then was filtered to remove insolubles. The filtrate was evaporated in vacuo, and purified by a column of SiO2 (50 ml) to give 248 mg (35.5%) of the title compound. Mp. 96.5°~98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04500526 |
| Source dataset | uspto-grants-1985_02 |
| ORD ID | ord-f7302cb7e27d494285267dc5dac02766 |
| Source note | uspto-grants-1985_02 |