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Water → 1-(4,6-Bis(dimethylamino)pyrimidin-2-yl)piperazine

HRID 1282182
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반응식

HRID 1282182 반응식
C([N:4]1[CH2:9][CH2:8][N:7]([C:10]2[N:15]=[C:14]([N:16]([CH3:18])[CH3:17])[CH:13]=[C:12]([N:19]([CH3:21])[CH3:20])[N:11]=2)[CH2:6][CH2:5]1)(=O)C.[OH-].[Na+].O>C(O)C>[CH3:17][N:16]([CH3:18])[C:14]1[CH:13]=[C:12]([N:19]([CH3:20])[CH3:21])[N:11]=[C:10]([N:7]2[CH2:8][CH2:9][NH:4][CH2:5][CH2:6]2)[N:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 184231391-Acetyl-4-(4,6-bis(dimethylamino)pyrimidin-2-yl)piperazine

생성물 1

HCID 184231011-(4,6-Bis(dimethylamino)pyrimidin-2-yl)piperazine수율 80.9%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 1-acetyl-4-(4,6-bis(dimethylamino)pyrimidin-2-yl)piperazine (1.3 g) and sodium hydroxide (0.5 g) in ethanol (15 ml)—water (15 ml) was refluxed under heating for 9.5 hr. The reaction mixture was concentrated under reduced pressure, and ethyl acetate was added to the residue and the mixture was washed with brine. The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated to give the title compound (0.9 g) as a pale-brown oil.

후처리

  1. temperatureunder heating for 9.5 hr
  2. concentrationThe reaction mixture was concentrated under reduced pressure, and ethyl acetate
  3. additionwas added to the residue
  4. washthe mixture was washed with brine
  5. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  6. customthe solvent was evaporated

출처 및 근거

ORD 기록
ord-a1b0cbb35a3a42fca2892d7884be8c98
출처 데이터셋
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06455528B1

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