Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 61456Generated: October 31, 2026

Dichloromethane → (3s,5s,6s)-5-(Methoxycarbonyl)-1-methyl-6-[(4-phenyl-3,6-dihydropyridin-1(2h)-yl)carbonyl]piperidin-3-yl piperidine-1-carboxylate

https://huagongshe.com/reaction/61456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPiperidineHCID 8082—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantMethyl (2s,3s,5s)-5-hydroxy-1-methyl-2-[(4-phenyl-3,6-dihydropyridin-1(2h)-yl)carbonyl]piperidine-3-carboxylateHCID 67304114—
Product(3s,5s,6s)-5-(Methoxycarbonyl)-1-methyl-6-[(4-phenyl-3,6-dihydropyridin-1(2h)-yl)carbonyl]piperidin-3-yl piperidine-1-carboxylateHCID 67304225—

Reaction Steps

A solution of methyl(2S,3S,5S)-5-hydroxy-1-methyl-2-[(4-phenyl-3,6-dihydropyridin-1(2H)-yl)carbonyl]piperidine-3-carboxylate (72 mg, 0.00020 mol) in methylene chloride (2.0 mL, 0.031 mol) was treated with N,N-carbonyldiimidazole (50 mg, 0.0003 mol) at rt for 2 h. To the mixture was added piperidine (0.060 mL, 0.00060 mol). After stirred at rt overnight, the mixture was concentrated to dry and used directly in next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440958B2
Source datasetuspto-grants-2016_09
ORD IDord-9313db97b17140319bef5b7980514fb1
Source noteuspto-grants-2016_09