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

HRID 1626311
Notes
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Reaction equation

HRID 1626311 reaction equation
[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
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Conditions

Temperature
90 °C

Procedure

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.

Workup

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

Sources & evidence

ORD record
ord-614e1a2d1e0344629e52805dc7c532a2
Source dataset
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08785453B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes