Reacción #313736

ord-bba8c3b4f7204b968a8a8fe865439841

Ecuación de reacción

Fc1cnc(Cl)nc1Nc1ccc2c(c1)OCCO2
2-chloro-N4-(3,4-ethylenedioxyphenyl)-5-fluoro-4-pyrimidineamine
Fc1cnc(Cl)nc1Cl
2,4-dichloro-5-fluoropyrimidine
Nc1cccc(CO)c1
3-aminobenzylalcohol
OCc1cccc(Nc2nc(Cl)ncc2F)c1
2-chloro-5-fluoro-N4-[3-(hydroxymethyl)phenyl]-4-pyrimidineamine

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowere reacted

Procedimiento

In a manner similar to the preparation of 2-chloro-N4-(3,4-ethylenedioxyphenyl)-5-fluoro-4-pyrimidineamine, 2,4-dichloro-5-fluoropyrimidine and 3-aminobenzylalcohol were reacted to yield 2-chloro-5-fluoro-N4-[3-(hydroxymethyl)phenyl]-4-pyrimidineamine. 1H NMR (CDCl3): δ 8.45 (bs, 1H), 7.96 (d, 1H, J=2.9 Hz), 7.65 (d, 1H, J=8.2 Hz), 7.34 (s, 1H), 7.31 (t, 1H, J=8.2 Hz), 7.07 (d, 1H, J=8.2), 4.52 (s, 2H)); 19F NMR (CDCl3): −44394 (s, 1F); LCMS: ret. time: 20.29 min.; purity: 100%; MS (m/e): 254 (MH+).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07557210B2uspto-grants-2009_07