HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → phenyl 6,7-dihydro-5H-cyclopenta[b]pyridin-3-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 5H,6H,7H-cyclopenta[b]pyridin-3-amine | HCID 10630532 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | phenyl 6,7-dihydro-5H-cyclopenta[b]pyridin-3-ylcarbamate | HCID 86676321 | — |
Reaction Steps
6,7-Dihydro-5H-cyclopenta[b]pyridin-3-amine (D) (250 mg, 1.86 mmol) was dissolved in acetonitrile. The reaction mixture was added pyridine (0.18 mL, 2.23 mmol) and phenyl chloroformate (0.26 mL, 2.05 mmol) and stirred at room temperature for 3 h 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 6,7-dihydro-5H-cyclopenta[b]pyridin-3-ylcarbamate (E). (372 mg, 78%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029378B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-89fb5b9d7633410faa025e4b9a90a699 |
| Source note | uspto-grants-2015_05 |