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1-Methylpiperazine → 2-Isocyano-1-(4-methylpiperazin-1-yl)ethanone

HRID 2065841
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HRID 2065841 반응식
[N+:1]([CH2:3][C:4]([O:6]C)=O)#[C-:2].[CH3:8][N:9]1[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]1>>[N+:1]([CH2:3][C:4]([N:12]1[CH2:13][CH2:14][N:9]([CH3:8])[CH2:10][CH2:11]1)=[O:6])#[C-:2]
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참가 물질

3

반응물 2

HCID 531671-MethylpiperazineHCID 547815Methyl isocyanoacetate

생성물 1

HCID 1819132-Isocyano-1-(4-methylpiperazin-1-yl)ethanone수율 99%

실험 절차

Prepared in accordance with Method B with methyl isocyanoacetate (1.0 g, 10.09 mmol) and N-methylpiperazine (1.37 mL, 15.14 mmol). The reaction mixture was stirred overnight at RT and then concentrated. The residue was dissolved in dichloromethane (50 mL) and evaporated. The residue was coevaporated three times with a mixture of CH2Cl2:cyclohexane=50:50 (3×10 mL). After drying 2-isocyano-1-(4-methyl-piperazin-1-yl)-ethanone VIB 01128 was obtained as yellow solid (1.67 g, 99% yield).

후처리

  1. concentrationconcentrated
  2. dissolutionThe residue was dissolved in dichloromethane (50 mL)
  3. customevaporated
  4. additionwith a mixture of CH2Cl2
  5. dry with materialAfter drying 2-isocyano-1-(4-methyl-piperazin-1-yl)-ethanone VIB 01128

출처 및 근거

ORD 기록
ord-dd4134985667492ab88b59d1c0e34cd9
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08288556B2

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