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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695956Generated: November 2, 2026

tert-butyl 4-(2-(N-methoxy-N-methylcarbamoyl)-6-fluorophenyl)-5,6-dihydropyridine-1(2H)-carboxylate → tert-Butyl 4-(2-(N-methoxy-N-methylcarbamoyl)-6-fluorophenyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1695956

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-(2-(N-methoxy-N-methylcarbamoyl)-6-fluorophenyl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 57774426—
CatalystAdams' catalystHCID 345198—
SolventEthanolHCID 702—
Producttert-Butyl 4-(2-(N-methoxy-N-methylcarbamoyl)-6-fluorophenyl)piperidine-1-carboxylateHCID 57774380—

Reaction Steps

A solution of tert-butyl 4-(2-(N-methoxy-N-methylcarbamoyl)-6-fluorophenyl)-5,6-dihydropyridine-1(2H)-carboxylate (450 mg, 1.235 mmol) and PtO2 (180 mg) in EtOH (19 mL) was shaken in a Parr flask for 1 h15 under 51 psi of H2. The reaction was monitored by LC/MS. Unreacted SM was detected, so another 150 mg of PtO2 (total: 450 mg, 30 wt %) was then added and the mixture was hydrogenated under 50 psi for another 3 h. Mostly desired product was detected after 4 h by LC/MS (Rt=2.83 min). The catalyst was filtered off and the solution was concentrated in vacuo to yield 435 mg of tert-butyl 4-(2-(N-methoxy-N-methylcarbamoyl)-6-fluorophenyl)piperidine-1-carboxylate as a clear thick oil which was used as is for the next step. LC/MS ES+1: 367.38.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163737B2
Source datasetuspto-grants-2012_04
ORD IDord-086d53ecf2bb4e56bdc4a8d37d640eec
Source noteuspto-grants-2012_04