1,4-Dioxane hydrochloride → 4-{2-[5-(4-Acetylpiperazin-1-yl)pyridin-2-yl]ethyl}benzyl hydrazinecarboxylate trihydrochloride

HRID 1465475노트

반응식

HRID 1465475 반응식
[NH:1]([C:10]([O:12][CH2:13][C:14]1[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][C:22]2[CH:27]=[CH:26][C:25]([N:28]3[CH2:33][CH2:32][N:31]([C:34](=[O:36])[CH3:35])[CH2:30][CH2:29]3)=[CH:24][N:23]=2)=[CH:16][CH:15]=1)=[O:11])[NH:2]C(OC(C)(C)C)=O.O1CCOCC1.[ClH:43]>ClCCl>[ClH:43].[ClH:43].[ClH:43].[NH:1]([C:10]([O:12][CH2:13][C:14]1[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][C:22]2[CH:27]=[CH:26][C:25]([N:28]3[CH2:33][CH2:32][N:31]([C:34](=[O:36])[CH3:35])[CH2:30][CH2:29]3)=[CH:24][N:23]=2)=[CH:16][CH:15]=1)=[O:11])[NH2:2]

참가 물질

4

실험 절차

To a suspension of 4-{2-[5-(4-acetylpiperazin-1-yl)pyridin-2-yl]ethyl}benzyl tert-butyl hydrazine-1,2-dicarboxylate (139.2 mg, 0.2797 mmol) in anhydrous dichloromethane (1.4 ml) was added 4M hydrogen chloride dioxane solution (1.4 ml, 5.6 mmol). After stirring at room temperature for 8 hrs, the mixture was concentrated under reduced pressure. Ethyl acetate was added to the concentrated residue, and the mixture was concentrated again under reduced pressure. The operation was repeated twice to azeotropically remove hydrogen chloride gas. The residue was dissolved in ethanol (6 ml), and ethyl acetate (30 ml) was added. The precipitated solid was filtered and dried under reduced pressure to give the title compound (105.3 mg, yield 74.3%) as a slightly yellow solid.

후처리

  1. concentrationthe mixture was concentrated under reduced pressure
  2. additionEthyl acetate was added to the concentrated residue
  3. concentrationthe mixture was concentrated again under reduced pressure
  4. dissolutionThe residue was dissolved in ethanol (6 ml)
  5. additionethyl acetate (30 ml) was added
  6. filtrationThe precipitated solid was filtered
  7. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-90793235085f4258a6184f471a2769d4
출처 데이터셋
uspto-grants-2015_04
특허 번호
US08999989B2

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