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Sodium Chloride → 1-(5-Cyclopropyl-3-methylpyridin-2-yl)piperazine

HRID 1804043
ノート
印刷プレビュー

反応式

HRID 1804043 の反応式
Cl.[CH:2]1([C:5]2[CH:6]=[C:7]([CH3:17])[C:8]([N:11]3[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]3)=[N:9][CH:10]=2)[CH2:4][CH2:3]1.C(OCC)(=O)C.[OH-].[Na+].[Cl-].[Na+]>O>[CH:2]1([C:5]2[CH:6]=[C:7]([CH3:17])[C:8]([N:11]3[CH2:12][CH2:13][NH:14][CH2:15][CH2:16]3)=[N:9][CH:10]=2)[CH2:4][CH2:3]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 5234Sodium ChlorideHCID 8857Ethyl AcetateHCID 14798Sodium HydroxideHCID 673810911-(5-Cyclopropyl-3-methylpyridin-2-yl)piperazine hydrochloride

生成物 1

HCID 584847181-(5-Cyclopropyl-3-methylpyridin-2-yl)piperazine

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To 1-(5-cyclopropyl-3-methylpyridin-2-yl)piperazine hydrochloride described in Preparation Example 49 was added ethyl acetate (50 mL), 1N aqueous sodium hydroxide solution (10 mL) was added under cooling and the mixture was stirred. To the reaction mixture were added sodium chloride and water under cooling, and the mixture was extracted twice with ethyl acetate. The organic layer was dried over sodium sulfate. The solvent was evaporated under reduced pressure to give the title compound (1.43 g).

後処理

  1. additionwas added
  2. temperatureunder cooling
  3. temperatureunder cooling
  4. extractionthe mixture was extracted twice with ethyl acetate
  5. dry with materialThe organic layer was dried over sodium sulfate
  6. customThe solvent was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-db679c82dc974dbca2e4717fe69527da
出典データセット
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08354401B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート