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Acetic Acid → HCID 23329856, compound

HRID 1447880
Notes
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Reaction equation

HRID 1447880 reaction equation
C[N:2]([CH3:17])[CH:3]=[CH:4][C:5]([C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([C:13]([F:16])([F:15])[F:14])[CH:8]=1)=O.[NH2:18][C:19]1[N:20]=[CH:21][NH:22][C:23]=1C#N.[C:26](O)(=O)C>>[CH3:26][C:3]1[CH:4]=[C:5]([C:7]2[CH:8]=[C:9]([C:13]([F:14])([F:15])[F:16])[CH:10]=[CH:11][CH:12]=2)[N:20]2[CH:21]=[N:22][C:23]([C:19]#[N:18])=[C:17]2[N:2]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 176Acetic AcidHCID 787775-amino-1H-imidazole-4-carbonitrileHCID 7300243-Dimethylamino-3'-trifluoromethylacrylophenone

Product 1

HCID 23329856HCID 23329856, compound

Procedure

A mixture of 0.01 mole of 3-dimethylamino-3'-(trifluoromethyl)acrylophenone, 50 ml. of glacial acetic acid and 0.01 mole of 4-amino-5-imidazolecarbonitrile is refluxed for 5 hours. The solvent is removed under reduced pressure and the residue worked up as for Example 29 to give the product of the example.

Workup

  1. customThe solvent is removed under reduced pressure
  • customto give the product of the example
  • Sources & evidence

    ORD record
    ord-cd76b40de25b451294820b24e35cf563
    Source dataset
    uspto-grants-1979_12
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04178449

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes