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Ethylamine → HCID 67274438, compound

HRID 1163336
Notes
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Reaction equation

HRID 1163336 reaction equation
[C:1]1([CH2:7][N:8]2[CH2:13][CH2:12][N:11]([CH2:14][C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[CH2:10][CH:9]2[CH:21]=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:23]([NH2:25])[CH3:24]>ClCCl>[CH2:7]([N:8]1[CH2:13][CH2:12][N:11]([CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:10][CH:9]1[CH:21]=[N:25][CH2:23][CH3:24])[C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 6341EthylamineHCID 154809991,4-Dibenzylpiperazine-2-carbaldehyde

Product 1

HCID 67274438HCID 67274438, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of 0.5 g (1,4-bis(phenylmethyl)-2-piperazin-carboxaldehyd in 5 ml of dichloromethane was added 0.54 ml ethylamine and 0.5 g molecular sieves. The reaction mixture was stirred for 30 min at rt then filtered. The filtrate was evaporated to dryness.

Workup

  1. filtration
then filtered
  • customThe filtrate was evaporated to dryness
  • Sources & evidence

    ORD record
    ord-1871d8010f5e496384cb4e83ed620633
    Source dataset
    uspto-grants-2010_10
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07820823B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes