Hydrochloric Acid → 4-Amino-2-(methylsulfanyl)pyrimidine-5-carbaldehyde

HRID 270704

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HRID 270704 반응식
[NH2:1][C:2]1[C:7]([C:8]#N)=[CH:6][N:5]=[C:4]([S:10][CH3:11])[N:3]=1.[H-].C([Al+]CC(C)C)C(C)C.Cl.C([O-])([O-])=[O:24].[Na+].[Na+]>C1COCC1>[NH2:1][C:2]1[C:7]([CH:8]=[O:24])=[CH:6][N:5]=[C:4]([S:10][CH3:11])[N:3]=1

참가 물질

6

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온도
0 °C

실험 절차

To a solution of 4-amino-2-(methylthio)pyrimidine-5-carbonitrile (3.0 g, 18.05 mmol) in THF (100 mL) is added diisobutylaluminum hydride (41.52 mL, 1.0 M in CH2Cl2, 41.52 mmol) at 0° C. After the mixture is stirred for 2.5 hours at 0° C., hydrochloric acid (2N, 30 mL) is added and stirring is continued for 20 minutes. To the reaction mixture is added saturated Na2CO3 until a pH of 8 is achieved. The suspended material is filtered through Celit pad and washed with K2CO3 solution. The solution is diluted with EtOAc and washed with saturated K2CO3, brine and dried, filtered and concentrated to give crude product, which is purified by flash silica gel column, eluting with hexane (100%) gradient to hexane/ether (60/40%), to give the title intermediate as a solid (1.62 g, 53.1%).

후처리

  1. stirringstirring
  2. waitis continued for 20 minutes
  3. filtrationThe suspended material is filtered through Celit pad
  4. washwashed with K2CO3 solution
  5. additionThe solution is diluted with EtOAc
  6. washwashed with saturated K2CO3, brine
  7. customdried
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customto give crude product, which
  11. customis purified by flash silica gel column
  12. washeluting with hexane (100%) gradient to hexane/ether (60/40%)

출처 및 근거

ORD 기록
ord-4f82a12b8b6b4e0b823e207cd72b0dda
출처 데이터셋
uspto-grants-2008_11
특허 번호
US07449582B2

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