関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Iodide | HCID 4875 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 2-(4-Methoxyphenyl)ethyl methanesulfonate | HCID 277977 | — |
| 反応物 | N-(4-piperidinyl)-2-benzothiazolamine dihydrobromide | HCID 14575275 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | N-[1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]-2-benzothiazolamine | HCID 14575764 | 41% |
反応手順
A mixture of 2.3 parts of [2-(4-methoxyphenyl)ethyl] methanesulfonate, 4 parts of N-(4-piperidinyl)-2-benzothiazolamine dihydrobromide, 5.3 parts of sodium carbonate, 0.1 parts of potassium iodide and 90 parts of N,N-dimethylformamide was stirred overnight at 70° C. The reaction mixture was poured onto water and the product was extracted with methylbenzene. The extract was washed with water, dried, filtered and evaporated. The residue was crystallized from a mixture of 2-propanol and 2,2'-oxybispropane. The product was filtered off and dried, yielding 1.5 parts (41%) of N-[1-[2-(4-methoxyphenyl)-ethyl]-4-piperidinyl]-2-benzothiazolamine; mp. 142.5° C. (178).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05010198 |
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| 出典データセット | uspto-grants-1991_04 |
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| ORD ID | ord-2b99b01b32df4e46b27ab0a7d10c157d |
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| 出典メモ | uspto-grants-1991_04 |
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