Reaktion #710473

ord-bcb4421405d34698b8aef0a94d9dfd49

Reaktionsgleichung

O=C(O)C(F)F
difluoroacetic acid
CCN=C=NCCCN(C)C.Cl
EDC-HCl
Nc1ccccn1
2-aminopyridine
O=C(N=c1cccc[nH]1)C(F)F
2,2-difluoro-N-(pyridin-2(1H)-ylidene)acetamide
Ausbeute 14.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed once with water and twice with a 1% HCl aqueous solution
  2. 2
    Trocknendried over anhydrous magnesium sulfate
  3. 3
    Einengenconcentrated under reduced pressure

Vorschrift

400 mg (4.26 mmol) of 2-aminopyridine was dissolved in 10 ml of anhydrous dichloromethane, 322 μl (490 mg, 5.11 mmol) of difluoroacetic acid, 982 mg (5.10 mmol) of EDC-HCl and 622 mg (5.11 mmol) of DMAP were added thereto, and the resulting mixture was stirred at room temperature for 61 hours. After the reaction was completed, the reaction solution was diluted with dichloromethane, washed once with water and twice with a 1% HCl aqueous solution, and then dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain 102 mg (yield 14%) of 2,2-difluoro-N-(pyridin-2(1H)-ylidene)acetamide.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09301525B2uspto-grants-2016_04