반응식
[OH-].[Na+].C[O:4][C:5](=[O:30])[C:6]1[CH:11]=[CH:10][C:9]([S:12]([N:15]2[C:23]3[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=3)[C:17]([CH:24]3[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]3)=[CH:16]2)(=[O:14])=[O:13])=[CH:8][CH:7]=1.Cl>C1COCC1.CO.CCOC(C)=O>[CH:24]1([C:17]2[C:18]3[C:23](=[CH:22][CH:21]=[CH:20][CH:19]=3)[N:15]([S:12]([C:9]3[CH:10]=[CH:11][C:6]([C:5]([OH:30])=[O:4])=[CH:7][CH:8]=3)(=[O:14])=[O:13])[CH:16]=2)[CH2:25][CH2:26][CH2:27][CH2:28][CH2:29]1참가 물질
7
실험 절차
Add 5N sodium hydroxide (1.17 ml, 3 eq) to a solution of 4-(3-Cyclohexyl-indole-1-sulfonyl)-benzoic acid methyl ester (775 mg, 1.95 mmol, 1 eq) dissolve in a mixture of 10 ml THF and 5 ml MeOH. Stir for 1.5 hours. Remove solvent on rotovap and add 1 N HCl. Dissolve the solid that crashes out of solution in EtOAc. Extract product into organics, separate organics, dry over MgSO4, and concentrate on rotovap to give 4-(3-Cyclohexyl-indole-1-sulfonyl)-benzoic acid (646 mg, 86% yield) as a white solid.
후처리
- customExtract product into organics, separate organics
- dry with materialdry over MgSO4
- concentrationconcentrate on rotovap
출처 및 근거
- ORD 기록
- ord-8c7886b322944d85ae586b50243955a4
- 출처 데이터셋
- uspto-grants-2007_10
- 특허 번호
- US07276516B2
연결된 노트
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