Nitrogen → 4-Bromo-1-phenyl-1H-pyrazole

HRID 219252

반응식

HRID 219252 반응식
[Br:1][C:2]1[CH:3]=[N:4][NH:5][CH:6]=1.I[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.N[C@@H]1CCCC[C@H]1N.C(=O)([O-])[O-].[K+].[K+].N#N>CCOC(C)=O.[Cu](I)I.O1CCOCC1>[Br:1][C:2]1[CH:3]=[N:4][N:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=1

참가 물질

9

실험 절차

A sealable tube was charged with 4-bromopyrazole (4.000 g, 27.2 mmol), 1-iodobenzene (3.64 ml, 32.7 mmol), (+/−)-trans-1,2-diaminocyclohexane (0.654 ml, 5.44 mmol), Copper iodide (I) (0.518 g, 2.72 mmol), potassium carbonate (8.28 g, 59.9 mmol) and 13 mL dioxane added. The mixture was blanketed with N2, the vessel sealed and heated to 100 C for 16 h. The mixture was allowed to cool to rt, diluted with EtOAc, washed with water, and an emulsion formed. The organic layer separated and the aqueous emulsion mixture was filter through a pad of celite and rinsed with EtOAc, and sat. NaHCO3. The combined organic layers were dried over Na2SO4, filtered and evaporate. The mixture was purified via flash chromatography using a 0% to 100% CH2Cl2 in hexanes gradient. The title compound was collected as a yellow solid (3.18 g)

후처리

  1. additionadded
  2. customthe vessel sealed
  3. temperatureheated to 100 C for 16 h
  4. washwashed with water
  5. customan emulsion formed
  6. customThe organic layer separated
  7. filtrationthe aqueous emulsion mixture was filter through a pad of celite
  8. washrinsed with EtOAc, and sat. NaHCO3
  9. dry with materialThe combined organic layers were dried over Na2SO4
  10. filtrationfiltered
  11. customevaporate
  12. customThe mixture was purified via flash chromatography
  13. customThe title compound was collected as a yellow solid (3.18 g)

출처 및 근거

ORD 기록
ord-8f97bf32e8f04275b1d828d896252d2f
출처 데이터셋
uspto-grants-2012_06
특허 번호
US08198448B2

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