HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → phenyl 1H-pyrazolo[3,4-b]pyridin-5-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 1-Methyl-3,5-dinitro-1H-pyridin-2-one | HCID 3621236 | — |
| Product | phenyl 1H-pyrazolo[3,4-b]pyridin-5-ylcarbamate | HCID 86676322 | — |
Reaction Steps
1H-Pyrazolo[3,4-b]pyridin-5-amine (B) (212 mg, 1.58 mmol) was dissolved in acetonitrile. To the reaction mixture was added pyridine (0.15 mL, 1.896 mmol) and phenyl chloroformate (0.2 mL, 1.659 mmol) and stirred at room temperature for 30 min under N2. TLC showed complete consumption of starting material. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic part was washed with water and brine. The organic layer was dried over MgSO4 and concentrated under reduced pressure. The crude was purified by column chromatography to give phenyl 1H-pyrazolo[3,4-b]pyridin-5-ylcarbamate (C). (285 mg, 71%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029378B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-deeb550db3d74083a74d75ce34b3fe80 |
| Source note | uspto-grants-2015_05 |