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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571979Generated: October 30, 2026

Pyridine → phenyl 6,7-dihydro-5H-cyclopenta[b]pyridin-3-ylcarbamate

https://huagongshe.com/reaction/571979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenyl chloroformateHCID 15891—
Reactant5H,6H,7H-cyclopenta[b]pyridin-3-amineHCID 10630532—
SolventAcetonitrileHCID 6342—
Productphenyl 6,7-dihydro-5H-cyclopenta[b]pyridin-3-ylcarbamateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029378B2
Source datasetuspto-grants-2015_05
ORD IDord-89fb5b9d7633410faa025e4b9a90a699
Source noteuspto-grants-2015_05