Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 225971생성일: 2026년 10월 26일
Diisopropylcarbodiimide → (3Ez,5s)-1-(biphenyl-4-ylcarbonyl)-5-[(3-methyl-1,2,4oxadiazol-5-yl)methyl]pyrrolidin-3-one o-methyloxime
https://huagongshe.com/reaction/225971
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylcarbodiimide | HCID 12734 | — |
| 반응물 | N-Hydroxyacetamidine | HCID 30926 | — |
| 반응물 | [(2S,4EZ)-1-(biphenyl-4-ylcarbonyl)-4-(methoxyimino)pyrrolidin-2-yl] acetic acid | HCID 131727525 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (3Ez,5s)-1-(biphenyl-4-ylcarbonyl)-5-[(3-methyl-1,2,4oxadiazol-5-yl)methyl]pyrrolidin-3-one o-methyloxime | HCID 131727534 | 102.4% |
반응 단계
To a solution of [(2S,4EZ)-1-biphenyl-4-ylcarbonyl)-4-(methoxyimino)pyrrolidin-2-yl]acetic acid (Intermediate 7, 50 mg, 0.14 mmol) in dichloromethane (3 ml) was added N′-hydroxyethanimidamide (12 mg, 0.16 mmol) followed by DIC (36 mg, 0.28 mmol). The reaction mixture was stirred 1 h30. The precipitate was filtered and the solution was concentrated in vacuo. Pyridine (1 ml) was added and the reaction mixture was stirred at reflux overnight The solvent was removed and dichloromethane was added. The organic phase was washed with HCl 1N then NaHCO3. The organic phase was dried (MgSO4), concentrated and purified on silica gel column chromatography (Ethyl acetate/cyclohexane, 40:60) to afford (3EZ,5S)-1-(biphenyl-4-ylcarbonyl)-5-[(3-methyl-1,2,4oxadiazol-5-yl)methyl]pyrrolidin-3-one O-methyloxime (56 mg). Yield: 91%. HPLC purity: 90%
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07557136B2 |
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| 출처 데이터셋 | uspto-grants-2009_07 |
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| ORD ID | ord-0ac680e44b2a4b5faab3f1a675f39c0c |
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| 출처 메모 | uspto-grants-2009_07 |
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