Water → 6-Bromo-2-(4-methanesulfonyl-benzyl)-7-methyl-8-(3-trifluoromethyl-phenyl)-2H-[1,2,4]triazolo[4,3-a]pyridin-3-one

HRID 1497767노트

반응식

HRID 1497767 반응식
[Br:1][C:2]1[C:3]([CH3:22])=[C:4]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([C:18]([F:21])([F:20])[F:19])[CH:13]=2)[C:5]2[N:6]([C:8](=[O:11])[NH:9][N:10]=2)[CH:7]=1.C(=O)([O-])[O-].[Cs+].[Cs+].[CH3:29][S:30]([C:33]1[CH:40]=[CH:39][C:36]([CH2:37]Br)=[CH:35][CH:34]=1)(=[O:32])=[O:31].O>CN(C=O)C>[Br:1][C:2]1[C:3]([CH3:22])=[C:4]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([C:18]([F:20])([F:19])[F:21])[CH:13]=2)[C:5]2[N:6]([C:8](=[O:11])[N:9]([CH2:37][C:36]3[CH:35]=[CH:34][C:33]([S:30]([CH3:29])(=[O:32])=[O:31])=[CH:40][CH:39]=3)[N:10]=2)[CH:7]=1

참가 물질

6

실험 절차

To a solution of 6-bromo-7-methyl-8-(3-trifluoromethyl-phenyl)-2H-[1,2,4]triazolo[4,3-a]pyridin-3-one (Int. 15, 55 mg, 0.148 mmol) in DMF (3 mL) was added cesium carbonate (58 mg, 0.177 mmol) followed by 4-(methylsulfonyl)benzyl bromide (40 mg, 0.163 mmol) and the mixture was stirred at RT for 20 hrs. Further amounts of cesium carbonate (25 mg) and 4-(methylsulfonyl)benzyl bromide (20 mg) were added and stirring was continued for 2 hrs. Water was added and the mixture was extracted with EtOAc (2×25 mL). The combined organic extracts were washed with brine then dried (Na2SO4), filtered and evaporated in vacuo. The resultant residue was purified by flash chromatography, eluting with a gradient of 0-100% EtOAc in cyclohexane to give the title compound as a yellow solid (49 mg).

후처리

  1. stirringstirring
  2. waitwas continued for 2 hrs
  3. extractionthe mixture was extracted with EtOAc (2×25 mL)
  4. washThe combined organic extracts were washed with brine
  5. dry with materialthen dried (Na2SO4)
  6. filtrationfiltered
  7. customevaporated in vacuo
  8. customThe resultant residue was purified by flash chromatography
  9. washeluting with a gradient of 0-100% EtOAc in cyclohexane

출처 및 근거

ORD 기록
ord-ac09267342804ac6994b94ebc79103f0
출처 데이터셋
uspto-grants-2015_12
특허 번호
US09199984B2

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