Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Cvt-2738 | HCID 2608606 | — |
| Reactant | HCID 18630841 | HCID 18630841 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 86619163 | HCID 86619163 | 10% |
| Product | HCID 86619164 | HCID 86619164 | 12% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE037886E1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-8884a82ccd264e8ba4eb91024956d4c8 |
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| Source note | uspto-grants-2002_10 |
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