반응식
C(=O)([O-])[O-].[Cs+].[Cs+].[CH2:7]([O:9][C:10]1[CH:11]=[C:12]([OH:16])[CH:13]=[CH:14][CH:15]=1)[CH3:8].Br[C:18]1[CH:23]=[CH:22][C:21]([N:24]2[C:28]([CH3:29])=[N:27][NH:26][C:25]2=[O:30])=[CH:20][CH:19]=1.CC(C)(C(=O)CC(=O)C(C)(C)C)C>CN1C(=O)CCC1.[Cu](Cl)Cl>[CH2:7]([O:9][C:10]1[CH:11]=[C:12]([O:16][C:18]2[CH:19]=[CH:20][C:21]([N:24]3[C:28]([CH3:29])=[N:27][NH:26][C:25]3=[O:30])=[CH:22][CH:23]=2)[CH:13]=[CH:14][CH:15]=1)[CH3:8]참가 물질
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
To cesium carbonate (641 mg, 1.968 mmol, 2 equiv) was added 3-ethoxyphenol (272 mg, 1.968 mmol, 2 equiv) in 4 mL of NMP. The reaction mixture was degassed and filled with nitrogen 3 times (3 cycles vacuum/nitrogen). 4-(4-bromophenyl)-5-methyl-2,4-dihydro-3H-1,2,4-triazol-3-one (Intermediate 22, 250 mg, 0.984 mg, 1 equiv), 2,2,6,6-tetramethyl-3,5-heptanedione (18 mg, 0.098 mmol, 0.1 equiv) and copper chloride (58 mg, 0.590 mmol, 0.6 equiv) were added. The reaction mixture was degassed and filled with nitrogen 3 times (3 cycles vacuum/nitrogen) and then warmed to 120 C under nitrogen overnight. The reaction mixture was diluted with dichloromethane and filtered. Volatiles were removed in vacuo and the residue was purified by preparative HPLC to give the title compound (20.2 mg).
후처리
- customThe reaction mixture was degassed
- additionfilled with nitrogen 3 times (3 cycles vacuum/nitrogen)
- customThe reaction mixture was degassed
- additionfilled with nitrogen 3 times (3 cycles vacuum/nitrogen)
- temperaturewarmed to 120 C under nitrogen overnight
- additionThe reaction mixture was diluted with dichloromethane
- filtrationfiltered
- customVolatiles were removed in vacuo
- customthe residue was purified by preparative HPLC
출처 및 근거
- ORD 기록
- ord-2ac0da37bd484d5bae3e0c3966ac3876
- 출처 데이터셋
- uspto-grants-2016_08
- 특허 번호
- US09422252B2
연결된 노트
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