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Dimethylamine → N4,N4,6-Trimethyl-2,4-pyridinediamine

HRID 1504778
Notes
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Reaction equation

HRID 1504778 reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([CH3:8])[CH:5]=[C:4](Cl)[CH:3]=1.[CH3:10][NH:11][CH3:12]>>[CH3:10][N:11]([CH3:12])[C:4]1[CH:5]=[C:6]([CH3:8])[N:7]=[C:2]([NH2:1])[CH:3]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 674DimethylamineHCID 190505094-Chloro-6-methylpyridin-2-amine

Product 1

HCID 667547N4,N4,6-Trimethyl-2,4-pyridinediamine

Conditions

Temperature
130 °C

Procedure

To 6-amino-4-chloro-2-picoline (500 mg, 3.51 mmol) in a vial under nitrogen was added dimethylamine (40% in water, 17.5 ml, 35.0 mmol). The reaction mixture was sealed and heated at 130° C. in a microwave for 2.5 hours. The reaction mixture was cooled, concentrated under reduced pressure, and purified by silica gel chromatography (2-10% methanol/DCM with 1% ammonium hydroxide, linear gradient) to give N4,N4,6-trimethylpyridine-2,4-diamine. MS ESI calc'd. for C8H14N3 [M+H]+ 152. found 152. 1H NMR (500 MHz, DMSO-d6) δ 6.15 (s, 2H), 6.02 (s, 1H), 5.54 (s, 1H), 2.90 (s, 6H), 2.18 (s, 3H).

Workup

  • customThe reaction mixture was sealed
  • temperatureThe reaction mixture was cooled
  • concentrationconcentrated under reduced pressure
  • custompurified by silica gel chromatography (2-10% methanol/DCM with 1% ammonium hydroxide, linear gradient)
  • Sources & evidence

    ORD record
    ord-be7d9f75d3f14dc0aa52d055fcf08d76
    Source dataset
    uspto-grants-2015_12
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US09216173B2

    Reaction notes

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    On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes