반응식
[CH2:1]([O:3][C:4]([C@H:6]1[CH2:8][C@@H:7]1[C:9]1[CH:14]=[CH:13][C:12]([O:15][C@H:16]2[C:24]3[C:19](=[C:20]([C:29]4[CH:34]=[CH:33][C:32]([OH:35])=[CH:31][CH:30]=4)[C:21]([C:25]([F:28])([F:27])[F:26])=[CH:22][CH:23]=3)[CH2:18][CH2:17]2)=[CH:11][CH:10]=1)=[O:5])[CH3:2].[O:36]1[C:38]2([CH2:43][CH2:42][O:41][CH2:40][CH2:39]2)[CH2:37]1.C(=O)([O-])[O-].[Cs+].[Cs+].Cl>CN(C)C=O.O>[CH2:1]([O:3][C:4]([C@H:6]1[CH2:8][C@@H:7]1[C:9]1[CH:10]=[CH:11][C:12]([O:15][C@H:16]2[C:24]3[C:19](=[C:20]([C:29]4[CH:34]=[CH:33][C:32]([O:35][CH2:37][C:38]5([OH:36])[CH2:43][CH2:42][O:41][CH2:40][CH2:39]5)=[CH:31][CH:30]=4)[C:21]([C:25]([F:26])([F:27])[F:28])=[CH:22][CH:23]=3)[CH2:18][CH2:17]2)=[CH:13][CH:14]=1)=[O:5])[CH3:2]참가 물질
7
반응 조건
- 온도
- 100 °C
실험 절차
((1S,2S)-2-{4-[(R)-4-(4-Hydroxy-phenyl)-5-trifluoromethyl-indan-1-yloxy]-phenyl}-cyclopro-panecarboxylic acid ethyl ester (crude from step 2), 1,6-dioxa-spiro[2.5]octane (US2012/46304, 44 mg) and cesium carbonate (198 mg) are suspended in dry N,N-dimethylformamide and heated at 100° C. for 3 hours. The mixture is diluted with water, acidified with 0.2 M HCl solution and extracted with ethyl acetate. The combined organic extracts are concentrated under vacuum and the residue purified by flash chromatography (0-30% EtOAc in cyclohexane) ti give the title compound (yield 50 mg).
후처리
- extractionextracted with ethyl acetate
- concentrationThe combined organic extracts are concentrated under vacuum
- customthe residue purified by flash chromatography (0-30% EtOAc in cyclohexane) ti
출처 및 근거
- ORD 기록
- ord-2ef9da7c07234a1bbac33a7b94f0ad9d
- 출처 데이터셋
- uspto-grants-2014_01
- 특허 번호
- US08633182B2
연결된 노트
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