反应 #1885081

ord-808fec0e973a46d6a631317af1d73ff5

反应方程式

CCOC(=O)c1cnc2ccccc2c1Cl
3a
CCOC(=O)c1cnc2ccccc2c1Cl
Ethyl 4-chloro-quinoline-3-carboxylate
CCOC(=O)c1cnc2cc(F)c(F)cc2c1O
2c
CCOC(=O)c1cnc2cc(F)c(F)cc2c1O
Ethyl 6,7-difluoro-4-hydroxy-quinoline-3-carboxylate
CCOC(=O)c1cnc2cc(F)c(F)cc2c1Cl
title compound
CCOC(=O)c1cnc2cc(F)c(F)cc2c1Cl
Ethyl 4-chloro-6,7-difluoro-quinoline-3-carboxylate

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

The title compound was prepared following the procedure described in Step 2 for the synthesis of 3a using 2c instead of 2a. 1H NMR (CDCl3) δ (ppm): 1.47 (3H, t, J=7.08 Hz), 4.56 (2H, q, J=7.08 Hz), 7.72 (1H, d, J=8.79 Hz), 8.39 (1H, d, J=8.78 Hz), 9.23 (1H, s). m/z 271.6/273.6 (M+/M+2). m/z 272.6(MH+).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08343957B2uspto-grants-2013_01