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

HRID 1804043
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HRID 1804043 반응식
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
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참가 물질

6

반응물 4

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

생성물 1

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

시약·촉매·용매 1

HCID 962Water용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-db679c82dc974dbca2e4717fe69527da
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08354401B2

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