Pyridine → HCID 9801397, 화합물

HRID 2307847노트

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HRID 2307847 반응식
NOS(O)(=O)=O.C[N:8](C)[C:9](=[N:11][C:12]([C:14]1[CH:15]=[N:16][C:17]([N:20]2[CH2:25][CH2:24][N:23]([C:26]3[CH:31]=[CH:30][CH:29]=[C:28]([C:32]([F:35])([F:34])[F:33])[CH:27]=3)[CH2:22][CH2:21]2)=[CH:18][CH:19]=1)=[S:13])[CH3:10].N1C=CC=CC=1>CO.C(O)C>[CH3:10][C:9]1[N:11]=[C:12]([C:14]2[CH:19]=[CH:18][C:17]([N:20]3[CH2:25][CH2:24][N:23]([C:26]4[CH:31]=[CH:30][CH:29]=[C:28]([C:32]([F:35])([F:34])[F:33])[CH:27]=4)[CH2:22][CH2:21]3)=[N:16][CH:15]=2)[S:13][N:8]=1

참가 물질

6

실험 절차

A mixture of hydroxylamine-O-sulfonic acid (0.011 mol) in methanol (15 ml) was added at once to a mixture of intermediate 5 (0.01 mol) and pyridine (0.02 mol) in ethanol (40 ml). The mixture was stirred at room temperature for 90 minutes. The solvent was evaporated. The residue was dissolved in DCM, washed with water and an aqueous NaOH 0.1N solution, dried, filtered and the solvent was evaporated. The residue was taken up in methanol, filtered off and dried. The residue was taken up in acetonitrile (100 ml). The mixture was stirred and boiled until complete dissolution and then allowed to crystallize out. The precipitate was filtered off and dried, yielding 1.4 g (35%) of 1-[5-(3-methyl-1,2,4-thiadiazol-5-yl)-2-pyridinyl]-4-[3-(trifluoromethyl)-phenyl]piperazine (compound 8).

후처리

  1. additionwas added at
  2. customThe solvent was evaporated
  3. dissolutionThe residue was dissolved in DCM
  4. washwashed with water
  5. dry with materialan aqueous NaOH 0.1N solution, dried
  6. filtrationfiltered
  7. customthe solvent was evaporated
  8. filtrationfiltered off
  9. customdried
  10. stirringThe mixture was stirred
  11. dissolutionboiled until complete dissolution
  12. customto crystallize out
  13. filtrationThe precipitate was filtered off
  14. customdried

출처 및 근거

ORD 기록
ord-6496cbdeb7114be4b8dab9009863131a
출처 데이터셋
uspto-grants-2004_12
특허 번호
US06833369B2

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