Acetic Acid → 1-{5-[5-(3,4-dichloro-phenyl)-1H-imidazol-2-yl]-pyridin-2-yl}-4-isobutyl-piperazine

HRID 276774

반응식

HRID 276774 반응식
C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].[Cl:15][C:16]1[CH:17]=[C:18]([C:23]2[N:24]=[C:25]([C:28]3[CH:29]=[CH:30][C:31]([N:34]4[CH2:39][CH2:38][NH:37][CH2:36][CH2:35]4)=[N:32][CH:33]=3)[NH:26][CH:27]=2)[CH:19]=[CH:20][C:21]=1[Cl:22].C(O)(=O)C.[CH:44](=O)[CH:45]([CH3:47])[CH3:46]>C1COCC1.[OH-].[Na+].C(OCC)(=O)C>[Cl:15][C:16]1[CH:17]=[C:18]([C:23]2[NH:24][C:25]([C:28]3[CH:29]=[CH:30][C:31]([N:34]4[CH2:39][CH2:38][N:37]([CH2:44][CH:45]([CH3:47])[CH3:46])[CH2:36][CH2:35]4)=[N:32][CH:33]=3)=[N:26][CH:27]=2)[CH:19]=[CH:20][C:21]=1[Cl:22]

참가 물질

8

실험 절차

Sodium triacetoxyborohydride (20.2 g) was added to a suspension of 1-{5-[4-(3,4-dichloro-phenyl)-1H-imidazol-2-yl]-pyridin-2-yl}-piperazine (23.8 g), acetic acid (5.1 mL), and isobutyraldehyde (6.35 mL) in THF (250 mL). The resultant suspension was stirred at ambient temperature for 18 hours, and then the reaction mixture was diluted with 1 N NaOH (1000 mL) and ethyl acetate (450 mL). The layers were separated, and the organic phase was diluted with hexanes (1000 mL). The resultant precipitate was collected by filtration, and the mother liquors were concentrated to 400 mL. The second crop of precipitate was collected and combined with the first crop to provide 1-{5-[5(3,4,-dichloro-phenyl)-1H-imidazol-2-yl]-pyridin-2-yl}-4-isobutyl-piperazine (22.5 g).

후처리

  1. customThe layers were separated
  2. additionthe organic phase was diluted with hexanes (1000 mL)
  3. filtrationThe resultant precipitate was collected by filtration
  4. concentrationthe mother liquors were concentrated to 400 mL
  5. customThe second crop of precipitate was collected

출처 및 근거

ORD 기록
ord-f668ec788e3840d7b5efe71c30b22f9b
출처 데이터셋
uspto-grants-2002_03
특허 번호
US06355635B1

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