반응식
[S:1]1[CH:5]=[CH:4][C:3]2[CH:6]=[CH:7][CH:8]=[CH:9][C:2]1=2.[CH2:10]([Li])[CH2:11][CH2:12][CH3:13].[CH3:15][O:16][C:17]1[CH:22]=[CH:21][C:20]([CH2:23][CH2:24][N:25]2[CH2:30][CH2:29][CH:28]([C:31]([O:33]C)=O)[CH2:27][CH2:26]2)=[CH:19][CH:18]=1>O1CCCC1>[CH3:15][O:16][C:17]1[CH:18]=[CH:19][C:20]([CH2:23][CH2:24][N:25]2[CH2:26][CH2:27][CH:28]([C:31]([C:10]3[S:1][C:2]4[CH:3]=[CH:4][CH:5]=[CH:13][C:12]=4[CH:11]=3)([C:5]3[S:1][C:2]4[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=4[CH:4]=3)[OH:33])[CH2:29][CH2:30]2)=[CH:21][CH:22]=1참가 물질
반응물 3
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- -78 °C
실험 절차
Dissolve benzo[b]thiophene(10.0 g, 74.5 mmol) in anhydrous tetrahydrofuran (100 mL), place under an argon atmosphere and cool to -78° C. Add, by dropwise addition, n-butyllithium (32.79 mL, 81.97 mmol) and stir briefly. Add, by dropwise addition, a solution of 1-[2-(4-methoxyphenyl)ethyl]-4-piperidinecarboxylic acid, methyl ester (20.67 g, 74.52 mmol) in anhydrous tetrahydrofuran (200 mL) and stir at -78° C. for 1.5 hours. Quench with saturated ammonium chloride, separate the organic phase and extract the aqueous phase with ethyl ether. Combine the organic phases, dry (MgSO4) and evaporate the solvent in vacuo. Purify by chromatography (50% ethyl acetate/hexane) and recrystallize (isopropanol) to give the title compound as a white solid; mp 168°-179° C.
후처리
- additionAdd, by dropwise addition
- customQuench with saturated ammonium chloride
- customseparate the organic phase
- extractionextract the aqueous phase with ethyl ether
- dry with materialdry (MgSO4)
- customevaporate the solvent in vacuo
- customPurify by chromatography (50% ethyl acetate/hexane)
- customrecrystallize (isopropanol)
출처 및 근거
- ORD 기록
- ord-63c5ab7c8d7743c2856cab6293760712
- 출처 데이터셋
- uspto-grants-1997_02
- 특허 번호
- US05602147
연결된 노트
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