反应 #84065

ord-fdc47d94f1cb47239575a8bc12e2a82d

反应方程式

Oc1ccc2nc(Cl)ccc2c1
2-chloroquinolin-6-ol
Oc1ccc2nc(Cl)ccc2c1
Intermediate 2
Oc1ccc2nc(Cl)ccc2c1
2-chloroquinolin-6-ol
O=C(O)c1ccc(B(O)O)cc1F
4-borono-2-fluorobenzoic acid
O=C(O)c1ccc(-c2ccc3cc(O)ccc3n2)cc1F
2-fluoro-4-(6-hydroxyquinolin-2-yl)benzoic acid

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Followed Scheme 3: Starting Materials: 2-chloroquinolin-6-ol (Intermediate 2) and 4-borono-2-fluorobenzoic acid. 1H NMR (CD3OD, 400 MHz): δ 8.54 (d, J=8.4 Hz, 1H), 8.20-8.06 (m, 3H), 8.06-7.96 (m, 2H), 7.55 (dd, J=9.2, 2.4 Hz, 1H), 7.32 (d, J=2.8 Hz, 1H). MS (ESI): m/z 283.6 [M+1]+.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09433618B2uspto-grants-2016_09