Sodium Carbonate → 3-bromo-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrimidine

HRID 1255867노트

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HRID 1255867 반응식
[Br:1][C:2]1[CH:3]=[N:4][N:5]2[CH:10]=[C:9](Br)[CH:8]=[N:7][C:6]=12.[CH3:12][N:13]1[CH:17]=[C:16](B2OC(C)(C)C(C)(C)O2)[CH:15]=[N:14]1.O1CCOCC1.C([O-])([O-])=O.[Na+].[Na+]>C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.O>[Br:1][C:2]1[CH:3]=[N:4][N:5]2[CH:10]=[C:9]([C:16]3[CH:15]=[N:14][N:13]([CH3:12])[CH:17]=3)[CH:8]=[N:7][C:6]=12

참가 물질

7

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온도
85 °C

실험 절차

3,6-Dibromopyrazolo[1,5-a]pyrimidine (2.0 g, 7.22 mmol) was mixed with 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (1.51 g, 7.22 mmol). Dioxane (36 mL) and 1M Na2CO3 (10.8 mL) were added. The mixture was evacuated and flushed with nitrogen under stirring, then Pd(Ph3P)4 (0.42 g, 0.36 mmol) was added in a counter flow of nitrogen. The reaction mixture was heated to 85° C. under stirring for 16 h, cooled, and poured into a 5-fold excess of water. The product was extracted thrice with CH2Cl2. The organic layer was washed with brine, dried with MgSO4, filtered, and evaporated. The residue was purified by column chromatography (1-5% methanol/DCM) to give 3-bromo-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrimidine as a yellow solid: LC/MS [M+H]=277.9.

후처리

  1. customThe mixture was evacuated
  2. customflushed with nitrogen
  3. stirringunder stirring for 16 h
  4. temperaturecooled
  5. extractionThe product was extracted thrice with CH2Cl2
  6. washThe organic layer was washed with brine
  7. dry with materialdried with MgSO4
  8. filtrationfiltered
  9. customevaporated
  10. customThe residue was purified by column chromatography (1-5% methanol/DCM)

출처 및 근거

ORD 기록
ord-15e25948bf3d4d1697fb888c584f19da
출처 데이터셋
uspto-grants-2013_06
특허 번호
US08461162B2

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