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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829178Generated: October 30, 2026

Piperidine → Ammonia

https://huagongshe.com/reaction/1829178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantPotassium CarbonateHCID 11430—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantTert-butyl 3-iodoazetidine-1-carboxylateHCID 11000522—
ProductAmmoniaHCID 222—
ProductHCID 22061396HCID 22061396—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of the piperidine from preparation 26 (220 mg, 1.91 mmol), tert-butyl 3-iodo-1-azetidinecarboxylate (600 mg, 2.0 mmol) (EP 992493) and potassium carbonate (276 mg, 2.0 mmol) in 1-methyl-2-pyrrolidinone (10 ml) was stirred at 80° C. for 48 hours. The mixture was partitioned between water and ethyl acetate, and the layers separated. The organic phase was washed with water, then brine, dried (Na2SO4), and evaporated under reduced pressure. The crude product was purified by column chromatography on silica gel using an elution gradient of dichloromethane:methanol:0.88 ammonia (100:0:0 to 90:10:0.5) to afford the title compound, 162 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060836B2
Source datasetuspto-grants-2006_06
ORD IDord-0319bc5ac6dc4d409c1dc9aab191b572
Source noteuspto-grants-2006_06