참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Ethane, 1-chloro-2-ethoxy- | HCID 12341 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 1-(3,4,5-trimethoxybenzoyl)-3-(2-(4-(1H-benzimidazol-2-yl-amino)piperidin-1-yl)ethyl)-3-(3,4-dichlorophenyl)pyrrolidine | HCID 9874360 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Ethyl acetate methanol triethylamine | HCID 21980445 | — |
| 생성물 | N,N-diethylethanamine;methyl butanoate | HCID 131722484 | — |
반응 단계
Combine 1-(3,4,5-trimethoxybenzoyl)-3-(2-(4-(1H-benzimidazol-2-yl-amino)piperidin-1-yl)ethyl)-3-(3,4-dichlorophenyl)pyrrolidine (0.54 g, 0.82 mmol) and dimethylformamide (15 mL). Add sodium hydride (0.07 g, 60% in oil, 1.8 mmol). After 1 hour, add 2-chloroethyl ethyl ether (1 mL). Heat to 100° C. After 18 hours, cool to ambient temperature and dilute the reaction mixture with dichloromethane. Extract three times with water, dry the organic layer over Na2SO4, filter and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 25/75/1 methanol/ethyl acetate/triethylamine. Collect the product containing fractions, evaporate in vacuo to give a residue, and chromatograph on silica gel eluting with 20/80/0.5 methanol ethyl acetate/triethylamine to give the title compound: Rf=0.23 (silica gel, 30% methanol/ethyl acetate).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06211199B1 |
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| 출처 데이터셋 | uspto-grants-2001_04 |
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| ORD ID | ord-ba28978f1ed94c70867ed611c4592984 |
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| 출처 메모 | uspto-grants-2001_04 |
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