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Potassium Iodide → N-(4-chlorophenyl)-N-(1-cyclopentyl-4-piperidinyl)benzeneacetamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Iodide | HCID 4875 | — |
| 反応物 | Bromocyclopentane | HCID 8728 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | N-(4-Chlorophenyl)-N-4-piperidinylbenzeneacetamide | HCID 162188 | — |
| 生成物 | N-(4-chlorophenyl)-N-(1-cyclopentyl-4-piperidinyl)benzeneacetamide | HCID 20334078 | — |
反応手順
to a stirred and warm (40° C.) mixture of 5 parts of N-(4-chlorophenyl)-N-(4-piperidinyl)benzeneacetamide, 5 parts of sodium carbonate, a few crystals of potassium iodide and 200 parts of nbutanol is added 3.75 parts of bromocyclopentane and the whole is stirred and refluxed for 21h.30. Then a second portion of 5 parts of bromocyclopentane is added and stirring at reflux temperature is continued for another 30 hours. The reaction mixture is cooled, filtered and the filtrate is evaporated. The oily residue solidifies on triturating in 1,1'-oxybisethane. The solid product is filtered off and crystallized from 1,1'-oxybisethane, yielding 1.1 parts of N-(4-chlorophenyl)-N-(1-cyclopentyl-4-piperidinyl)benzeneacetamide; mp. 139.5° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04151286 |
| 出典データセット | uspto-grants-1979_04 |
| ORD ID | ord-0fb7ca53bca64e0fa512792348c1f012 |
| 出典メモ | uspto-grants-1979_04 |