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Methylamine → 2-(Methylamino)pyridine-3-carbonitrile

HRID 1723020
Notes
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Reaction equation

HRID 1723020 reaction equation
Cl[C:2]1[N:9]=[CH:8][CH:7]=[CH:6][C:3]=1[C:4]#[N:5].[CH3:10][NH2:11]>>[CH3:10][NH:11][C:2]1[N:9]=[CH:8][CH:7]=[CH:6][C:3]=1[C:4]#[N:5]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 6329MethylamineHCID 810792-Chloronicotinonitrile

Product 1

HCID 124571912-(Methylamino)pyridine-3-carbonitrile

Procedure

A solution of 2-chloronicotinonitrile (97.82 g, 706 mmol) in 40% aqueous methylamine (706 ml) was heated to reflux for 1.5 hour. The excess methylamine was evaporated off and the resulting solids filtered and washed with water (250 mL). The crude product was dissolved in boiling water (1.4 l) and treated with charcoal and filtered through Celite. The aqueous filtrate was cooled to room temperature. After 10 hours the crystalline solid was collected, washed with water and dried to leave 71.10 g of 2-(methylamino)-nicotinonitrile (mp. 86-88 degrees C.). A sample was further purified by sublimation (100 degrees C. at 0.025 mm) mp. (87-88 degrees C.).

Workup

  1. temperatureto reflux for 1.5 hour
  2. customThe excess methylamine was evaporated off
  3. filtrationthe resulting solids filtered
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
wash
washed with water (250 mL)
  • dissolutionThe crude product was dissolved
  • additiontreated with charcoal
  • filtrationfiltered through Celite
  • customAfter 10 hours the crystalline solid was collected
  • washwashed with water
  • customdried
  • Sources & evidence

    ORD record
    ord-ebeb90c690574b399ba7fe7a6bbe59d8
    Source dataset
    uspto-grants-1989_08
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04859672

    Reaction notes

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