반응식
[F:1][C:2]1[CH:16]=[CH:15][C:5]([CH2:6][O:7][C:8]2[CH:13]=[CH:12][NH:11][C:10](=[O:14])[CH:9]=2)=[CH:4][CH:3]=1.Br[C:18]1[CH:23]=[CH:22][C:21](/[CH:24]=[CH:25]/[CH2:26][OH:27])=[CH:20][CH:19]=1.C(=O)([O-])[O-].[K+].[K+].O.N>C(OCC)(=O)C.CN(C=O)C>[F:1][C:2]1[CH:16]=[CH:15][C:5]([CH2:6][O:7][C:8]2[CH:13]=[CH:12][N:11]([C:18]3[CH:23]=[CH:22][C:21](/[CH:24]=[CH:25]/[CH2:26][OH:27])=[CH:20][CH:19]=3)[C:10](=[O:14])[CH:9]=2)=[CH:4][CH:3]=1참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
반응 조건
- 온도
- 155 °C
실험 절차
A mixture of 4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one (1.10 g, 5.0 mmol), (2E)-3-(4-bromophenyl)-2-propen-1-ol (1.28 g, 6 mmol), cuprous iodide (476 mg, 3 mmol), potassium carbonate (829 mg, 6 mmol) and DMF (20 mL) was stirred overnight at 155° C. The reaction liquid was cooled to room temperature, then poured into ammonia water, and ethyl acetate was added for extraction. The organic layer was washed with water and saturated saline, and dried with anhydrous magnesium sulfate. The solvent was concentrated under reduced pressure, followed by purification by flash column chromatography (KP-Sil, hexane:ethyl acetate=1:1 to 0:1) to obtain the entitled compound (881 mg).
후처리
- customThe reaction liquid
- temperaturewas cooled to room temperature
- additionwas added for extraction
- washThe organic layer was washed with water and saturated saline
- dry with materialdried with anhydrous magnesium sulfate
- concentrationThe solvent was concentrated under reduced pressure
- customfollowed by purification by flash column chromatography (KP-Sil, hexane:ethyl acetate=1:1 to 0:1)
출처 및 근거
- ORD 기록
- ord-d8bc3e29064449df8c43fa1906e3655b
- 출처 데이터셋
- uspto-grants-2011_01
- 특허 번호
- US07875633B2
연결된 노트
불러오는 중…