5-(tert-butyl-dimethyl-silanyloxy)-1H-indole-2-carboxylic acid ethyl ester → 1-(2-tert-butoxycarbonylamino-ethyl)-5-(tert-butyl-dimethyl-silanyloxy)-1H-indole-2-carboxylic acid ethyl ester
반응식
[CH2:1]([O:3][C:4]([C:6]1[NH:7][C:8]2[C:13]([CH:14]=1)=[CH:12][C:11]([O:15][Si:16]([C:19]([CH3:22])([CH3:21])[CH3:20])([CH3:18])[CH3:17])=[CH:10][CH:9]=2)=[O:5])[CH3:2].CC(C)([O-])C.[K+].[C:29]([O:33][C:34]([N:36]1[CH2:40][CH2:39]OS1(=O)=O)=[O:35])([CH3:32])([CH3:31])[CH3:30]>CN(C)C=O>[CH2:1]([O:3][C:4]([C:6]1[N:7]([CH2:39][CH2:40][NH:36][C:34]([O:33][C:29]([CH3:32])([CH3:31])[CH3:30])=[O:35])[C:8]2[C:13]([CH:14]=1)=[CH:12][C:11]([O:15][Si:16]([C:19]([CH3:21])([CH3:20])[CH3:22])([CH3:18])[CH3:17])=[CH:10][CH:9]=2)=[O:5])[CH3:2]참가 물질
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
The solution of 7.0 g (21.9 mmol) 5-(tert-butyl-dimethyl-silanyloxy)-1H-indole-2-carboxylic acid ethyl ester in 60 mL N,N-dimethylformamide was cooled down to 0° C. and 2.7 g (24.1 mmol) potassium tert-butoxide was added. After 30 min., 5.4 g (24.2 mmol) 2,2-dioxo-[1,2,3]oxathiazolidine-3-carboxylic acid tert-butyl ester (prepared according to WO 02/072584) was added and the cooling bath was removed. After 1.5 hours, 10% aqueous ammonium chloride solution was added and the two-phase mixture was extracted twice with ethyl acetate. The combined organic layers were washed with water and brine, dried over magnesium sulfate, filtered and evaporated. The thus obtained crude product (brown oil; 12.0 g, 100%) was used without further purification for the next step.
후처리
- customthe cooling bath was removed
- waitAfter 1.5 hours
- addition10% aqueous ammonium chloride solution was added
- extractionthe two-phase mixture was extracted twice with ethyl acetate
- washThe combined organic layers were washed with water and brine
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- customevaporated
출처 및 근거
- ORD 기록
- ord-530054f56f964822a1cc88713fbe3a34
- 출처 데이터셋
- uspto-grants-2009_08
- 특허 번호
- US07579351B2
반응 노트
불러오는 중…