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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775348Generated: October 30, 2026

tert-Butyl 4-(2-methyl-3-pyridyl)-3,6-dihydro-2H-pyridine-1-carboxylate → tert-Butyl 4-(2-methyl-3-pyridyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1775348

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(2-methyl-3-pyridyl)-3,6-dihydro-2H-pyridine-1-carboxylateHCID 121257689—
SolventEthanolHCID 702—
SolventHCID 178418361HCID 178418361—
Producttert-Butyl 4-(2-methyl-3-pyridyl)piperidine-1-carboxylateHCID 13173473847.4%

Reaction Steps

tert-Butyl 4-(2-methyl-3-pyridyl)-3,6-dihydro-2H-pyridine-1-carboxylate (209 mg, 0.76 mmol) was dissolved in ethanol (42 ml) and hydrogenated in a H-cube hydrogen generator with a flow of 1 ml/min and at a temperature of 70° C. The mixture was evaporated under reduced pressure, the residue was purified by preparative HPLC (Waters X-Bridge, gradient of water containing 0.1% NH3 and acetonitrile) to yield 100 mg of a colourless solid (0.36 mmol, yield 47%). MS (ESI) m/z=277.2 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260441B2
Source datasetuspto-grants-2016_02
ORD IDord-b5f02792976a40629e93998750c1237b
Source noteuspto-grants-2016_02