Tetrahydrofuran → 5-[4-(cyclopropylsulfonyl)phenyl]-6-(tetrahydro-2H-pyran-4-yl)-1-[5-(2,2,2-trifluoro-1-hydroxyethyl)-1,3-thiazol-2-yl]hexane-1,4-dione
반응식
[CH:1]1([S:4]([C:7]2[CH:12]=[CH:11][C:10]([CH:13]([CH2:18][CH:19]3[CH2:24][CH2:23][O:22][CH2:21][CH2:20]3)[C:14](=[O:17])[CH:15]=[CH2:16])=[CH:9][CH:8]=2)(=[O:6])=[O:5])[CH2:3][CH2:2]1.[F:25][C:26]([F:37])([F:36])[CH:27]([C:29]1[S:33][C:32]([CH:34]=[O:35])=[N:31][CH:30]=1)[OH:28].C(N(CC)CC)C.O1CCCC1>[Cl-].C([N+]1C(C)=C(CCO)SC=1)C1C=CC=CC=1.C(O)C>[CH:1]1([S:4]([C:7]2[CH:8]=[CH:9][C:10]([CH:13]([CH2:18][CH:19]3[CH2:24][CH2:23][O:22][CH2:21][CH2:20]3)[C:14](=[O:17])[CH2:15][CH2:16][C:34]([C:32]3[S:33][C:29]([CH:27]([OH:28])[C:26]([F:36])([F:25])[F:37])=[CH:30][N:31]=3)=[O:35])=[CH:11][CH:12]=2)(=[O:6])=[O:5])[CH2:3][CH2:2]1참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
A mixture of 4-[4-(cyclopropylsulfonyl)phenyl]-5-(tetrahydro-2H-pyran-4-yl)pent-1-en-3-one (0.30 g), 5-(2,2,2-trifluoro-1-hydroxyethyl)-1,3-thiazole-2-carbaldehyde (0.20 g), 3-benzyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazol-3-ium chloride (23 mg), triethylamine (0.05 mL), tetrahydrofuran (4 mL) and ethanol (2 mL) was stirred with heating under reflux for 2 hr. The reaction mixture was concentrated, and the residue was subjected to silica gel column chromatography, and the title compound (0.45 g, yield 90%) was obtained as a colorless oil from a fraction eluted with ethyl acetate-hexane (4:1, volume ratio). MS: 560 (MH+).
후처리
- temperaturewith heating
- temperatureunder reflux for 2 hr
- concentrationThe reaction mixture was concentrated
출처 및 근거
- ORD 기록
- ord-ee488b30dd6b471eaa708629c422e01e
- 출처 데이터셋
- uspto-grants-2012_11
- 특허 번호
- US08318746B2
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