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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381089Generated: October 27, 2026

benzyl 4-[4-[3-(4-acetylpiperazin-1-yl)propoxy]phenyl]-5,6-dihydropyridine-1(2H)-carboxylate → 4-[4-[3-(4-Acetylpiperazin-1-yl)propoxy]phenyl]piperidine

https://huagongshe.com/reaction/2381089

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbenzyl 4-[4-[3-(4-acetylpiperazin-1-yl)propoxy]phenyl]-5,6-dihydropyridine-1(2H)-carboxylateHCID 68500054—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventIsopropanolHCID 3776—
SolventDichloromethaneHCID 6344—
ProductAmmoniaHCID 22210%
Product4-[4-[3-(4-Acetylpiperazin-1-yl)propoxy]phenyl]piperidineHCID 68504139152.9%

Reaction Steps

Benzyl 4-[4-[3-(4-acetylpiperazin-1-yl)propoxy]phenyl]-5,6-dihydropyridine-1(2H)-carboxylate (17 g, 35.59 mmol) and 5% palladium on carbon (3.37 g, 31.68 mmol) in iso-propanol (170 mL) were stirred under an atmosphere of hydrogen at 5 bar and 40° C. for 2 hours. The reaction mixture was filtered through diatomaceous earth, washing through with iso-propanol. The combined organics were evaporated to dryness to give crude product, which was purified by silica gel chromatography eluting with 0-10% MeOH in DCM, then 10% 7M ammonia in methanol in DCM, to give 4-[4-[3-(4-acetylpiperazin-1-yl)propoxy]phenyl]piperidine (9.4 g, 27.2 mmol, 76%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258140B2
Source datasetuspto-grants-2012_09
ORD IDord-b56b2272ff484e11b412ab75c264f005
Source noteuspto-grants-2012_09