反应 #1885085

ord-13a8c279e5f44daabbee66cb91fa2f38

反应方程式

CCOC(=O)c1cnc2ccc(C)cc2c1Cl
3f
CCOC(=O)c1cnc2ccc(C)cc2c1Cl
Ethyl 4-chloro-6-methyl-quinoline-3-carboxylate
NNc1ccccc1
phenyl hydrazine
Cc1ccc2[nH]cc3c(=O)n(-c4ccccc4)nc-3c2c1
title compound
Cc1ccc2[nH]cc3c(=O)n(-c4ccccc4)nc-3c2c1
8-Methyl-2-phenyl-2,5-dihydro-pyrazolo-(4,3-c)quinolin-3-one

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 3 using 3f and phenyl hydrazine. 1H NMR (DMSO-d6) δ (ppm): 2.46 (3H, s), 7.16 (1H, t, J=7.41 Hz), 7.41 (2H, dd, J=8.51, 7.14 Hz), 7.46 (1H, dd, J=8.52, 1.92 Hz), 7.58 (1H, d, J=8.51 Hz), 8.00 (1H, br), 8.21 (2H, dd, J=7.69, 1.10 Hz), 8.66 (1H, s). m/z 276.3 (MH+).

来源

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