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Methylamine → 4-(4-(2,3-Dimethylphenyl)piperazin-1-yl)-1-(methylamino)butan-2-ol

HRID 1626311
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인쇄 미리보기

반응식

HRID 1626311 반응식
[CH3:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1[N:9]1[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][CH:17]2[CH2:19][O:18]2)[CH2:11][CH2:10]1.[CH3:20][NH2:21]>C(O)C>[CH3:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1[N:9]1[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][CH:17]([OH:18])[CH2:19][NH:21][CH3:20])[CH2:11][CH2:10]1
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참가 물질

4

반응물 2

HCID 6329MethylamineHCID 866706301-(2,3-Dimethylphenyl)-4-(2-(oxiran-2-yl)ethyl)piperazine

생성물 1

HCID 672062844-(4-(2,3-Dimethylphenyl)piperazin-1-yl)-1-(methylamino)butan-2-ol

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
90 °C

실험 절차

A mixture of 1-(2,3-dimethylphenyl)-4-(2-(oxiran-2-yl)ethyl)piperazine obtained in step 2 (0.10 g, 0.38 mmol) and methylamine (8.0 M) in ethanol (1.0 ml) was stirred at 90° C. for 20 hours. After the reaction complete, the resulting reaction mixture was concentrated under reduced pressure to obtain the title compound (0.10 g). The compound was used for the next step without further purification.

후처리

  1. customAfter the reaction complete, the resulting reaction mixture
  2. concentrationwas concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-614e1a2d1e0344629e52805dc7c532a2
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08785453B2

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