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Methylamine → 3-Methoxy-N-methyl-4-(7H-purin-8-yl)benzamide

HRID 1380740
Notes
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Reaction equation

HRID 1380740 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([C:9]([NH2:11])=[O:10])[CH:6]=[CH:5][C:4]=1[C:12]1[NH:20][C:19]2[C:14](=[N:15][CH:16]=[N:17][CH:18]=2)[N:13]=1.[CH3:21]N>>[CH3:1][O:2][C:3]1[CH:8]=[C:7]([C:9]([NH:11][CH3:21])=[O:10])[CH:6]=[CH:5][C:4]=1[C:12]1[NH:20][C:19]2[C:14](=[N:15][CH:16]=[N:17][CH:18]=2)[N:13]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 6329MethylamineHCID 132845313-Methoxy-4-(7H-purin-8-yl)benzamide

Product 1

HCID 132845323-Methoxy-N-methyl-4-(7H-purin-8-yl)benzamide

Procedure

Forty milliliters of ethanolic methylamine solution were added to 0.42 gm of 8-(2'-methoxy-4'-chlorocarbonylphenyl)-purine hydrochloride (see Example 43), with cooling, and the mixture was refluxed for 30 minutes. It was then concentrated by evaporation, and the product was purified by column chromatography on silica gel [eluant: methylene chloride/ethanol (8:2)].

Workup

  1. temperaturewith cooling
  2. temperaturethe mixture was refluxed for 30 minutes
  3. concentrationIt was then concentrated by evaporation
  4. customthe product was purified by column chromatography on silica gel [eluant: methylene chloride/ethanol (8:2)]

Sources & evidence

ORD record
ord-a4137e4a4a544e069a63a7165fad9f9c
Source dataset
uspto-grants-1986_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04582837

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes