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

HRID 1465480ノート

反応式

HRID 1465480 の反応式
[C:1]([N:4]1[CH2:9][CH2:8][N:7]([C:10]2[CH:11]=[CH:12][C:13]([CH2:16][CH2:17][C:18]3[CH:36]=[CH:35][C:21]([CH2:22][NH:23][C:24]([NH:26][NH:27]C(OC(C)(C)C)=O)=[O:25])=[CH:20][CH:19]=3)=[N:14][CH:15]=2)[CH2:6][CH2:5]1)(=[O:3])[CH3:2].O1CCOCC1.[ClH:43]>O1CCOCC1>[ClH:43].[ClH:43].[ClH:43].[C:1]([N:4]1[CH2:9][CH2:8][N:7]([C:10]2[CH:11]=[CH:12][C:13]([CH2:16][CH2:17][C:18]3[CH:36]=[CH:35][C:21]([CH2:22][NH:23][C:24]([NH:26][NH2:27])=[O:25])=[CH:20][CH:19]=3)=[N:14][CH:15]=2)[CH2:6][CH2:5]1)(=[O:3])[CH3:2]

参加物

4

実験手順

To a suspension of tert-butyl 2-[(4-{2-[5-(4-acetylpiperazin-1-yl)pyridin-2-yl]ethyl}benzyl)carbamoyl]hydrazinecarboxylate (121.0 mg, 0.243 mmol) in anhydrous dioxane (1.2 ml) was added 4M hydrogen chloride dioxane solution (1.2 ml). After stirring at room temperature for 5 hrs, the reaction mixture was concentrated under reduced pressure. Ethyl acetate (10 ml) was added to the residue, and the mixture was concentrated again under reduced pressure. This operation was performed 3 times to azeotropically remove hydrogen chloride gas. The residue was suspended in a mixture of ethanol (3 ml) and ethyl acetate (6 ml), filtered, washed with ethyl acetate and dried under reduced pressure to give the title compound (111.0 mg, yield 90.1%) as a slightly yellow solid.

後処理

  1. concentrationthe reaction mixture was concentrated under reduced pressure
  2. additionEthyl acetate (10 ml) was added to the residue
  3. concentrationthe mixture was concentrated again under reduced pressure
  4. additionThe residue was suspended in a mixture of ethanol (3 ml) and ethyl acetate (6 ml)
  5. filtrationfiltered
  6. washwashed with ethyl acetate
  7. customdried under reduced pressure

出典と根拠

ORDレコード
ord-9309e39ea29346b19d937a61290bc583
出典データセット
uspto-grants-2015_04
特許番号
US08999989B2

反応ノート

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