Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564882Generated: October 30, 2026

Thiophene → (+/-)-1,1-Dimethylethyl 4-[4-(acetylamino)-4-phenyl-1-piperidinyl]-2-(phenylmethyl)-1-piperidinecarboxylate

https://huagongshe.com/reaction/564882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
ReactantN-(4-Phenylpiperidin-4-yl)acetamideHCID 15886675—
Reactant1-Boc-2-benzylpiperidin-4-oneHCID 18319921—
CatalystTitanium isopropoxideHCID 11026—
CatalystPlatinumHCID 23939—
SolventIsopropanolHCID 3776—
Product(+/-)-1,1-Dimethylethyl 4-[4-(acetylamino)-4-phenyl-1-piperidinyl]-2-(phenylmethyl)-1-piperidinecarboxylateHCID 1831992781.4%

Reaction Steps

A mixture of (±)-1,1-dimethylethyl 4-oxo-2-(phenylmethyl)-1-piperidine carboxylate (0.1 mol) and N-(4-phenyl-4-piperidinyl)acetamide (0.1 mol) in 2-propanol (500 ml) was hydrogenated at 50° C. with platinum (4 g) as a catalyst in the presence of titanium (IV)isopropoxide (28.5 g) and thiophene (4%; 1 ml). After uptake of hydrogen the catalyst was filtered off and the filtrate was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH 97/3). The pure fractions were collected and the solvent was evaporated, yielding 40 g (74.1% ) of (±)-1,1-dimethylethyl 4-[4-(acetylamino)-4-phenyl-1-piperidinyl]-2-(phenylmethyl)-1-piperidinecarboxylate (intermediate 19).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06169097A
Source datasetuspto-grants-2001_01
ORD IDord-415f39641d254f7095e45fb428ff75d9
Source noteuspto-grants-2001_01