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Hydrochloric Acid → 2,3,4,5-Tetrahydro-3-oxo-4-[(pyridin-3-yl)-methyleneamino]-6-methyl-1,2,4-triazinehydrochloride

HRID 2106642
Notes
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Reaction equation

HRID 2106642 reaction equation
[O:1]=[C:2]1[N:7]([N:8]=[CH:9][C:10]2[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=2)[CH2:6][C:5]([CH3:16])=[N:4][NH:3]1.[ClH:17]>>[ClH:17].[O:1]=[C:2]1[N:7]([N:8]=[CH:9][C:10]2[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=2)[CH2:6][C:5]([CH3:16])=[N:4][NH:3]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 313Hydrochloric AcidHCID 863704,5-Dihydro-6-methyl-4-((3-pyridinylmethylene)amino)-1,2,4-triazin-3(2H)-one

Product 1

HCID 679245022,3,4,5-Tetrahydro-3-oxo-4-[(pyridin-3-yl)-methyleneamino]-6-methyl-1,2,4-triazinehydrochloride

Procedure

21.7 g of 2,3,4,5-tetrahydro-3-oxo-4-[(pyridin-3-yl)-methyleneamino]-6-methyl-1,2,4-triazine are dissolved, with heating, in 60 ml of 2N hydrochloric acid. The hot solution is filtered and cooled. The precipitate which crystallises out is isolated by filtration, washed with alcohol and ether and dried in vacuo to give the title compound of formula ##STR32## in the form of a colourless crystal powder; m.p. 240-241° C. with decomposition; yield: 19 g (75%).

Workup

  1. filtrationThe hot solution is filtered
  • temperaturecooled
  • customThe precipitate which crystallises out
  • customis isolated by filtration
  • washwashed with alcohol and ether
  • customdried in vacuo
  • Sources & evidence

    ORD record
    ord-10518bb3c4774c4e8e131818f65ec661
    Source dataset
    uspto-grants-1990_06
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04931439

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes