참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Iodide | HCID 4875 | — |
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | 2-(4-Methoxyphenyl)ethyl methanesulfonate | HCID 277977 | — |
| 반응물 | N-(4-piperidinyl)-2-benzothiazolamine dihydrobromide | HCID 14575275 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-[1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]-2-benzothiazolamine | HCID 14575764 | 41% |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05010198 |
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| 출처 데이터셋 | uspto-grants-1991_04 |
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| ORD ID | ord-2b99b01b32df4e46b27ab0a7d10c157d |
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| 출처 메모 | uspto-grants-1991_04 |
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