Reaktion #1133160

ord-a186298a208b4f2ba8b464ac625f960a

Reaktionsgleichung

Cc1cc(Nc2cc(I)c(C(F)(F)F)cn2)n(C)n1
N-(1,3-dimethylpyrazol-5-yl)-4-iodo-5-(trifluoromethyl)pyridin-2-amine
CONC(=O)c1ccc(F)cc1N
2-amino-4-fluoro-N-methoxybenzamide
CONC(=O)c1ccc(F)cc1Nc1cc(Nc2cc(C)nn2C)ncc1C(F)(F)F
2-[[2-[(2,5-dimethylpyrazol-3-yl)amino]-5-(trifluoromethyl)-4-pyridyl]amino]-4-fluoro-N-methoxy-benzamide

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigetriturated in Et2O

Vorschrift

This compound was prepared from N-(1,3-dimethylpyrazol-5-yl)-4-iodo-5-(trifluoromethyl)pyridin-2-amine and 2-amino-4-fluoro-N-methoxybenzamide. 81 mg, 48%; triturated in Et2O; NMR Spectrum: (DMSOd6) 2.08 (s, 3H), 3.55 (s, 3H), 3.70 (s, 3H), 6.04 (s, 1H), 6.74 (s, 1H), 6.97 (ddd, 1H), 7.43 (dd, 1H), 7.66 (dd, 1H), 8.28 (s, 1H), 9.07 (s, 1H), 10.04 (bs, 1H), 11.96 (bs, 1H); Mass spectrum: MH+ 439.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08569298B2uspto-grants-2013_10