5-Bromo-N'-(chloroacetyl)-3-pyridinecarbohydrazide → 3-Bromo-5-[5-(chloromethyl)-1,3,4-oxadiazol-2-yl]pyridine

HRID 2101836노트

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HRID 2101836 반응식
[Br:1][C:2]1[CH:3]=[C:4]([C:8]([NH:10][NH:11][C:12](=[O:15])[CH2:13][Cl:14])=O)[CH:5]=[N:6][CH:7]=1>O=P(Cl)(Cl)Cl>[Br:1][C:2]1[CH:7]=[N:6][CH:5]=[C:4]([C:8]2[O:15][C:12]([CH2:13][Cl:14])=[N:11][N:10]=2)[CH:3]=1

참가 물질

3

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온도
110 °C

실험 절차

A suspension of 5-bromo-N′-(chloroacetyl)-3-pyridinecarbohydrazide (3.65 g, 12.48 mmol) in POCl3 (20 mL) was heated at 110° C. for 1.5 h. Upon cooling, the mixture was concentrated in vacuo. The residue was diluted with EtOAc and sat'd NaHCO3 solution was added slowly while stirring. The pH of the aqueous phase was adjusted to ˜8 by addition of sat'd K2CO3 solution. The phases were separated and the aqueous phase was extracted twice with EtOAc. The combined organic phases were washed with sat'd brine, dried (Na2SO4), and concentrated in vacuo. The residue was purified by flash chromatography (0-50% EtOAc-hexanes gradient) to afford the title compound as a light yellow solid (2.01 g, 59% yield): MS (ES) m/z 274 and 276 (M+1 Br isotopes).

후처리

  1. temperatureUpon cooling
  2. concentrationthe mixture was concentrated in vacuo
  3. additionThe residue was diluted with EtOAc
  4. additionwas added slowly
  5. additionThe pH of the aqueous phase was adjusted to ˜8 by addition of sat'd K2CO3 solution
  6. customThe phases were separated
  7. extractionthe aqueous phase was extracted twice with EtOAc
  8. washThe combined organic phases were washed with sat'd brine
  9. dry with materialdried (Na2SO4)
  10. concentrationconcentrated in vacuo
  11. customThe residue was purified by flash chromatography (0-50% EtOAc-hexanes gradient)

출처 및 근거

ORD 기록
ord-72ae83f20aae444a8b53081b4e86a7a7
출처 데이터셋
uspto-grants-2009_08
특허 번호
US07572820B2

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