تفاعل #7355

ord-81279442efa746b7a617ec2073a76c32

معادلة التفاعل

Oc1cc(Cl)c2nc(-c3ccc(O)c(F)c3)cc(Br)c2c1
45a
Oc1cc(Cl)c2nc(-c3ccc(O)c(F)c3)cc(Br)c2c1
4-Bromo-8-chloro-2-(3-fluoro-4-hydroxyphenyl)quinolin-6-ol
COc1ccc(B(O)O)cc1
4-methoxyphenylboronic acid
COc1ccc(-c2cc(-c3ccc(O)c(F)c3)nc3c(Cl)cc(O)cc23)cc1
8-Chloro-2-(3-fluoro-4-hydroxyphenyl)-4-(4-methoxyphenyl)quinolin-6-ol
المردود 97.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

الإجراء التجريبي

This compound was prepared from 45a using 4-methoxyphenylboronic acid according to method P. Orange solid; Yield: 97%; mp 140–142° C.; 1H-NMR (400 MHz, DMSO-d6) δ 3.87 (s, 3H), 7.09 (dd, J=8.8, 8.8 Hz, 1H), 7.11 (d, J=2.7 Hz, 1H), 7.16 (d, J=8.8 Hz, 2H), 7.51 (d, J=2.6 Hz, 1H), 7.53 (d, J=8.8 Hz, 2H), 7.93(s, 1H), 8.02 (dd, J=8.5, 1.7 Hz, 1H), 8.14 (dd, J=13.1, 2.1 Hz, 1H), 10.21 (s, 1H), 10.27 (s, 1H); 19F-NMR (400 MHz, DMSO-d6) δ −136.48 (dd, J=13.0, 9.7 Hz); MS (ESI) m/z 394/396 ([M−H]−), 396/398 ([M+H]+); Anal. Calcd for C22H15ClFNO3: C: 66.76, H: 3.82, N: 3.54. Found: C: 66.05, H: 4.01, N: 3.19.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07084276B2uspto-grants-2006_08