Cesium carbonate → 4-(4-{[3-(ethyloxy)phenyl]oxy}phenyl)-5-methyl-2,4-dihydro-3H-1,2,4-triazol-3-one

HRID 1484523

반응식

HRID 1484523 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

7

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

  1. customThe reaction mixture was degassed
  2. additionfilled with nitrogen 3 times (3 cycles vacuum/nitrogen)
  3. customThe reaction mixture was degassed
  4. additionfilled with nitrogen 3 times (3 cycles vacuum/nitrogen)
  5. temperaturewarmed to 120 C under nitrogen overnight
  6. additionThe reaction mixture was diluted with dichloromethane
  7. filtrationfiltered
  8. customVolatiles were removed in vacuo
  9. customthe residue was purified by preparative HPLC

출처 및 근거

ORD 기록
ord-2ac0da37bd484d5bae3e0c3966ac3876
출처 데이터셋
uspto-grants-2016_08
특허 번호
US09422252B2

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