HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167111Generated: October 25, 2026
Potassium Carbonate → Methyl 2-methyl-2-phenyl-6-{4-[(4'-trifluoromethyl-biphenyl-2-carbonyl)-amino]-piperidin-1-yl}-hexanecarboxylate
https://huagongshe.com/reaction/1167111
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(Piperidin-4-yl)-4'-(trifluoromethyl)-biphenyl-2-carboxamide | HCID 9928271 | — |
| Reactant | Methyl 6-bromo-2-methyl-2-phenyl-hexanecarboxylate | HCID 22995743 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 2-methyl-2-phenyl-6-{4-[(4'-trifluoromethyl-biphenyl-2-carbonyl)-amino]-piperidin-1-yl}-hexanecarboxylate | HCID 22995675 | — |
Reaction Steps
0.2 g (0.574 mmol) of 4′-trifluoromethyl-biphenyl-2-carboxylic acid-piperidin-4-yl-amide, 0.15 g (0.5 mmol) of methyl 6-bromo-2-methyl-2-phenyl-hexanecarboxylate and 0.083 g (0.6 mmol) of potassium carbonate are dissolved in 10 ml of acetonitrile. The mixture is stirred for 8 hours at 60° C. and for 14 hours at ambient temperature. Then the reaction mixture is poured onto water and extracted with ethyl acetate. The organic phase is dried over sodium sulphate and the solvent is distilled off in the rotary evaporator. After column chromatography on silica gel (eluant: dichloromethane/methanol=20:1) a highly viscous oil remains.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06617325B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-6cd803da8c144149904d0fa9c1848818 |
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| Source note | uspto-grants-2003_09 |
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