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(-)-1-(N-methylanthraniloyl)-proline → 10-methyl-2,3-dihydro-1H-pyrrolo[2,1-c][1,4]benzodiazepine-5,11(10H,11aH)-dione

HRID 917965
Notes
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Reaction equation

HRID 917965 reaction equation
[CH3:1][NH:2][C:3]1[C:4](=[CH:15][CH:16]=[CH:17][CH:18]=1)[C:5]([N:7]1[CH2:14][CH2:13][CH2:12][C@H:8]1[C:9](O)=[O:10])=[O:6]>O1CCCC1>[CH3:1][N:2]1[C:3]2[CH:18]=[CH:17][CH:16]=[CH:15][C:4]=2[C:5](=[O:6])[N:7]2[CH2:14][CH2:13][CH2:12][CH:8]2[C:9]1=[O:10]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 22791454(-)-1-(N-methylanthraniloyl)-proline

Product 1

HCID 985943610-methyl-2,3-dihydro-1H-pyrrolo[2,1-c][1,4]benzodiazepine-5,11(10H,11aH)-dione

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

A mixture of 24.8 g. of racemic 1-(N-methylanthraniloyl)proline and 21 g. of dicyclohexylcarbonyl diimide in 300 ml. of tetrahydrofuran is stirred at room temperature for 24 hours and then heated on the steam bath for 4 hours. The reaction mixture is filtered to remove the insoluble dicyclohexyl urea and the mother liquid is concentrated to recover the desired product, which is further purified by recrystallization from ethyl acetate.

Workup

  1. addition
A mixture of 24.8 g
  • temperatureheated on the steam bath for 4 hours
  • filtrationThe reaction mixture is filtered
  • customto remove the insoluble dicyclohexyl urea
  • concentrationthe mother liquid is concentrated
  • customto recover the desired product, which
  • customis further purified by recrystallization from ethyl acetate
  • Sources & evidence

    ORD record
    ord-6860e4264a474dbc89fdcdd0f4faeb94
    Source dataset
    uspto-grants-1976_07
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US03968230

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes