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Hydrochloric Acid → 3-Methoxy-4-(7H-purin-8-yl)benzamide

HRID 2309883
Notes
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Reaction equation

HRID 2309883 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([C:9]#[N:10])[CH:6]=[CH:5][C:4]=1[C:11]1[NH:19][C:18]2[C:13](=[N:14][CH:15]=[N:16][CH:17]=2)[N:12]=1.Cl.[OH-:21].[Na+]>>[CH3:1][O:2][C:3]1[CH:8]=[C:7]([C:9]([NH2:10])=[O:21])[CH:6]=[CH:5][C:4]=1[C:11]1[NH:19][C:18]2[C:13](=[N:14][CH:15]=[N:16][CH:17]=2)[N:12]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 132845293-Methoxy-4-(7H-purin-8-yl)benzonitrile

Product 1

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

Procedure

One gram of 8-(2'-methoxy-4'-cyano-phenyl)-purine was dissolved in 75 ml of 2N sodium hydroxide solution and refluxed for 15 minutes. Then, the mixture was acidified with hydrochloric acid, and the mixture precipitated was separated into its components by use of silica gel [eluant:methylene chloride/ethanol (7:3 to 1:1)].

Workup

  1. temperaturerefluxed for 15 minutes
  2. customthe mixture precipitated
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
  • customwas separated into its components by use of silica gel [eluant:methylene chloride/ethanol (7:3 to 1:1)]
  • Sources & evidence

    ORD record
    ord-46072a7ae601409092a8ae54ad079d8c
    Source dataset
    uspto-grants-1987_09
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04696931

    Reaction notes

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