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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991369Generated: November 1, 2026

Thiophene → HCID 86619164, compound

https://huagongshe.com/reaction/991369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
ReactantCvt-2738HCID 2608606—
ReactantHCID 18630841HCID 18630841—
CatalystTitanium isopropoxideHCID 11026—
CatalystPlatinumHCID 23939—
SolventIsopropanolHCID 3776—
ProductHCID 86619163HCID 8661916310%
ProductHCID 86619164HCID 8661916412%

Reaction Steps

A mixture of (±)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-[[3-fluoro-5-(trifluoromethyl) phenyl]methyl]-4-piperidinone (0.01 mol) and N-(2,6-dimethylphenyl)-1-piperazine-acetamide (0.01 mol) in 2-propanol (150 ml) was hydrogenated at 50° C. with platinum on activated carbon (55), 2 g) as a catalyst in the presence of titanium(IV)isopropoxide (2.84 g) and thiophene solution (1 ml). After uptake of hydrogen, the catalyst was filtered off and the filtrate was evaporated. The residue was taken up in CH2Cl2 and H2O. The organic layer was separated, washed several times with H2O, dried, filtered over dicalite and the solvent was evaporated. This fraction was purified by HPLC over silica gel (eluent: CH2Cl2/CH3OH 98/2). Two pure factions were collected and their solvents were evaporated. The residue was dried, yielding 0.72 g (10%) of (±)-cis-4-[1-[3,5-bis (trifluoromethyl)benzoyl]-2-[[3fluoro-5-(trifluoromethyl) phenyl]methyl]-4-piperidinyl]-N—(2,6-dimethylphenyl)-1-piperazineacetamide (compound 140 ) and 0.88 g (12%) of (±)-trans-4-[1-[3,5-bis(trifluoromethyl)benzoyl]-2-[[3-fluoro-5-(trifluoro-methyl) phenyl]methyl]-4-piperidinyl]-N—(2,6-dimethylphenyl)-1-piperazineacetamide (compound 141).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037886E1
Source datasetuspto-grants-2002_10
ORD IDord-8884a82ccd264e8ba4eb91024956d4c8
Source noteuspto-grants-2002_10