Pyridine → HCID 9801397, 화합물
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]=1참가 물질
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
- additionwas added at
- customThe solvent was evaporated
- dissolutionThe residue was dissolved in DCM
- washwashed with water
- dry with materialan aqueous NaOH 0.1N solution, dried
- filtrationfiltered
- customthe solvent was evaporated
- filtrationfiltered off
- customdried
- stirringThe mixture was stirred
- dissolutionboiled until complete dissolution
- customto crystallize out
- filtrationThe precipitate was filtered off
- customdried
출처 및 근거
- ORD 기록
- ord-6496cbdeb7114be4b8dab9009863131a
- 출처 데이터셋
- uspto-grants-2004_12
- 특허 번호
- US06833369B2
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