Reacción #423184

ord-2a26bb09207e445caf53603825a365eb

Ecuación de reacción

NC1=N[C@@]2(CO1)c1cc(Br)ccc1Oc1c2cc(Cl)nc1F
(S)-7-bromo-3-chloro-1-fluoro-5′H-spiro[chromeno[2,3-c]pyridine-5,4′-oxazol]-2′-amine
OB(O)c1cccnc1F
2-fluoropyridin-3-ylboronic acid
Cl.FC1(F)CCNCC1
4,4-difluoropiperidine hydrochloride
NC1=N[C@@]2(CO1)c1cc(-c3cccnc3F)ccc1Oc1c2cc(N2CCC(F)(F)C2)nc1F
title compound
NC1=N[C@@]2(CO1)c1cc(-c3cccnc3F)ccc1Oc1c2cc(N2CCC(F)(F)C2)nc1F
(S)-3-(4,4-difluoropyrrolidin-1-yl)-1-fluoro-7-(2-fluoropyridin-3-yl)-5′-H-spiro[chromeno[2,3-c]pyridine-5,4′-oxazol]-2′-amine

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroprepared by steps analogous to

Procedimiento

The title compound was synthesized by steps analogous to those described in method CC4 above, but using (S)-7-bromo-3-chloro-1-fluoro-5′H-spiro[chromeno[2,3-c]pyridine-5,4′-oxazol]-2′-amine (prepared by steps analogous to those described in Method BB33), 2-fluoropyridin-3-ylboronic acid and 4,4-difluoropiperidine hydrochloride.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08883782B2uspto-grants-2014_11