Reaktion #164654

ord-e1a31e7fa8f345a8b0fbe839f635251e

Reaktionsgleichung

Nc1ccc(Cl)c(Cl)c1
3,4-dichloroaniline
COC(=O)c1cnc(Cl)cn1
methyl 5-chloropyrazine-2-carboxylate
COC(=O)c1cnc(Nc2ccc(Cl)c(Cl)c2)cn1
methyl 5-(3,4-dichlorophenylamino)pyrazine-2-carboxylate
Ausbeute 51.1%

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled to room temperature
  2. 2
    Einengenconcentrated
  3. 3
    SonstigeThe residue was triturated with methanol
  4. 4
    Filtrationfiltered
  5. 5
    WaschenThe brown filter cake was washed with methanol
  6. 6
    Sonstigedried

Vorschrift

A mixture of 3,4-dichloroaniline (1.127 g, 6.95 mmol) and methyl 5-chloropyrazine-2-carboxylate (0.6 g, 3.48 mmol) in dioxane (32 mL) was heated at 100° C. for 7 days, then cooled to room temperature and concentrated. The residue was triturated with methanol and filtered. The brown filter cake was washed with methanol and dried to yield methyl 5-(3,4-dichlorophenylamino)pyrazine-2-carboxylate (0.53 g, 51%). 1H NMR (400 MHz, DMSO-d6) δ ppm 10.44 (1H, s), 8.81 (1H, d, J=1.26 Hz), 8.30 (1H, d, J=1.51 Hz), 8.21 (1H, d, J=2.26 Hz), 7.46-7.73 (2H, m), 3.58 (2H, s). LCMS: R.T.=4.07; [M+H]+=298.12.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08841301B2uspto-grants-2014_09