반응식
C[O:2][C:3](=O)[CH:4]([CH:23]([C:32]1[CH:37]=[CH:36][C:35]([O:38][CH2:39][C:40]2[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=2)=[CH:34][CH:33]=1)[NH:24][C:25]1[CH:30]=[CH:29][C:28]([F:31])=[CH:27][CH:26]=1)[CH2:5][CH2:6]C(OCC1C=CC=CC=1)C1C=CC(F)=CC=1.C[Si]([N-][Si](C)(C)C)(C)C.[Li+].Cl.[C:58]([O:61][CH2:62][CH3:63])(=O)[CH3:59]>O1CCCC1>[CH2:62]([O:61][CH:58]([C:59]1[CH:30]=[CH:29][C:28]([F:31])=[CH:27][CH:26]=1)[CH2:6][CH2:5][CH:4]1[CH:23]([C:32]2[CH:33]=[CH:34][C:35]([O:38][CH2:39][C:40]3[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=3)=[CH:36][CH:37]=2)[N:24]([C:25]2[CH:30]=[CH:29][C:28]([F:31])=[CH:27][CH:26]=2)[C:3]1=[O:2])[C:63]1[CH:6]=[CH:5][CH:4]=[CH:23][CH:32]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- -22.5 °C
실험 절차
10 gms of 5-Benzyloxy-2-[(4-benzyloxy-phenyl)-(4-fluoro-phenylamino)-methyl]-5-(4-fluoro-phenyl)-pentanoic acid methyl ester was dissolved in 500 ml of tetrahydrofuran and cool the reaction mass to −20 to −25° C. To the reaction mass 16 ml of 1M Lithium bis(trimethylsilyl)amide was added under nitrogen atmosphere and stirred for about 30 minutes. To the reaction mass 100 ml of 2 N hydrochloride solution was added at 20-25° C. Stirred the reaction mass by adding 150 ml of ethyl acetate and separated the organic layer. Washed the organic layer with water and dried over sodium sulphate. Distilled the solvent completely under reduced pressure at 50-55° C. to get 8.0 gms of 3-[3-Benzyloxy-3-(4-fluoro-phenyl)-propyl]-4-(4-benzyloxy-phenyl)-1-(4-fluoro-phenyl)-azetidin-2-one.
후처리
- stirringStirred the reaction mass
- customseparated the organic layer
- washWashed the organic layer with water
- dry with materialdried over sodium sulphate
- distillationDistilled the solvent completely under reduced pressure at 50-55° C.
출처 및 근거
- ORD 기록
- ord-b92fb61efef34c0f9d8b1e1b477d5ec4
- 출처 데이터셋
- uspto-grants-2016_07
- 특허 번호
- US09388440B2
연결된 노트
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