1,10-Phenanthroline → 2-(5-Bromo-2-pyridinyl)benzoxazole

HRID 521547

반응식

HRID 521547 반응식
Br[C:2]1[CH:8]=[CH:7][CH:6]=[CH:5][C:3]=1[NH2:4].[Br:9][C:10]1[CH:11]=[CH:12][C:13]([C:16](Cl)=[O:17])=[N:14][CH:15]=1.C([O-])([O-])=O.[Cs+].[Cs+].N1C2C(=CC=C3C=2N=CC=C3)C=CC=1>[Cu]I.C(Cl)Cl.O1CCOCC1>[Br:9][C:10]1[CH:11]=[CH:12][C:13]([C:16]2[O:17][C:2]3[CH:8]=[CH:7][CH:6]=[CH:5][C:3]=3[N:4]=2)=[N:14][CH:15]=1

참가 물질

8

반응 조건

온도
120 °C

실험 절차

A mixture of 2-bromoaniline (3.90 g, 22.7 mmol), 5-bromopyridine-2-carbonyl chloride (5.00 g, 22.7 mmol), Cs2CO3 (14.78 g, 45.36 mmol), 1,10-phenanthroline (0.409 g, 2.27 mmol), CuI (0.216 g, 1.13 mmol) and anhydrous 1,4-dioxane (40 mL) was degassed with argon for about 40 min while stirring. The stirring reaction mixture was then maintained under argon at about 120° C. for about 40 h. Upon completion, the reaction was cooled to RT and poured over CH2Cl2 (300 mL). The organics were then washed with sat. NaHCO3, H2O and brine, dried over MgSO4, filter and concentrated in vacuo. Purification of the crude product via flash chromatography (SiO2, 4:1 dichloromethane-hexanes) and subsequent recrystallization from hexanes afforded compound 11 (1.86 g, 30% yield) as colorless fibers.

후처리

  1. customwas degassed with argon for about 40 min
  2. customThe stirring reaction mixture
  3. temperatureUpon completion, the reaction was cooled to RT
  4. washThe organics were then washed with sat. NaHCO3, H2O and brine
  5. dry with materialdried over MgSO4
  6. filtrationfilter
  7. concentrationconcentrated in vacuo
  8. customPurification of the crude product

출처 및 근거

ORD 기록
ord-3c0af32c96b544d6aa712ca19029fe13
출처 데이터셋
uspto-grants-2016_05
특허 번호
US09328086B2

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