Réaction #1509585

ord-419c479ac24b45acafa306f3d3b45ef9

Équation de réaction

C/C(N)=C\C#N
(E)-3-amino-but-2-enenitrile
C#CC(=O)OC
propynoic acid methyl ester
c1ccc(-c2ccccc2)cc1.c1ccc(Oc2ccccc2)cc1
Dowtherm
Cc1[nH]c(=O)ccc1C#N
2-Methyl-6-oxo-1,6-dihydro-pyridine-3-carbonitrile

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurerefluxed for additional 1 h
  2. 2
    Autrewas rised to 230° C
  3. 3
    workup.DISTILLATIONDMF and MeOH were distilled off
  4. 4
    TempératureThe reaction mixture was cooled down
  5. 5
    workup.ADDITIONEtOAc (200 ml) was added
  6. 6
    Filtrationthe resulting crystals were filtered off
  7. 7
    Lavagewashed with EtOAc and ether affording the title compound (44.8 g, FP>250° C.)

Mode opératoire

A solution of (E)-3-amino-but-2-enenitrile (100 g) and propynoic acid methyl ester in DMF (200 ml) was stirred at 25° C. for 2 h and refluxed for additional 1 h. Dowtherm (100 ml) was added and the temperature was rised to 230° C. DMF and MeOH were distilled off. The reaction mixture was cooled down, EtOAc (200 ml) was added and the resulting crystals were filtered off and washed with EtOAc and ether affording the title compound (44.8 g, FP>250° C.).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: USRE045323E1uspto-grants-2015_01