Réaction #710475

ord-257a8f432d0c4ef5aa005a2342a2e2f5

Équation de réaction

Nc1ccccn1
2-aminopyridine
CCN=C=NCCCN(C)C.Cl
EDC-HCl
O=C(O)C(F)(F)Cl
chlorodifluoroacetic acid
O=C(N=c1cccc[nH]1)C(F)(F)Cl
2-chloro-2,2-difluoro-N-(pyridin-2(1H)-ylidene)acetamide
Rendement 24.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Lavagewashed with water and 1% hydrochloric acid
  2. 2
    Séchagedried over anhydrous magnesium sulfate

Mode opératoire

200 mg (2.13 mmol) of 2-aminopyridine was dissolved in 5 ml of dichloromethane, 491 mg (2.55 mmol) of EDC-HCl, 311 mg (2.55 mmol) of DMAP and 187 μl (2.23 mmol, 290 mg) of chlorodifluoroacetic acid were added thereto in sequence, and the resulting mixture was stirred overnight. After the reaction was completed, the reaction solution was diluted with dichloromethane, washed with water and 1% hydrochloric acid, and then dried over anhydrous magnesium sulfate to obtain 105 mg (yield 24%) of 2-chloro-2,2-difluoro-N-(pyridin-2(1H)-ylidene)acetamide.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09301525B2uspto-grants-2016_04