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HRID 1167111作成日:2026年10月27日
Potassium Carbonate → Methyl 2-methyl-2-phenyl-6-{4-[(4'-trifluoromethyl-biphenyl-2-carbonyl)-amino]-piperidin-1-yl}-hexanecarboxylate
https://huagongshe.com/reaction/1167111
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | N-(Piperidin-4-yl)-4'-(trifluoromethyl)-biphenyl-2-carboxamide | HCID 9928271 | — |
| 反応物 | Methyl 6-bromo-2-methyl-2-phenyl-hexanecarboxylate | HCID 22995743 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | Methyl 2-methyl-2-phenyl-6-{4-[(4'-trifluoromethyl-biphenyl-2-carbonyl)-amino]-piperidin-1-yl}-hexanecarboxylate | HCID 22995675 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06617325B1 |
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| 出典データセット | uspto-grants-2003_09 |
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| ORD ID | ord-6cd803da8c144149904d0fa9c1848818 |
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| 出典メモ | uspto-grants-2003_09 |
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