反应 #1885089

ord-d664329faa5b4f7fa5abf36ff50b4b62

反应方程式

O=c1c2c[nH]c3ccccc3c-2nn1-c1ccccc1
4a
O=c1c2c[nH]c3ccccc3c-2nn1-c1ccccc1
2-Phenyl-2,5-dihydro-pyrazolo-(4,3-c) quinolin-3-one
CCOC(=O)c1cnc2ccc(C(F)(F)F)cc2c1Cl
3h
CCOC(=O)c1cnc2ccc(C(F)(F)F)cc2c1Cl
Ethyl 4-chloro-6-trifluoromethyl-quinoline-3-carboxylate
NNc1ccccc1
phenyl hydrazine
O=c1c2c[nH]c3ccc(C(F)(F)F)cc3c-2nn1-c1ccccc1
title compound
O=c1c2c[nH]c3ccc(C(F)(F)F)cc3c-2nn1-c1ccccc1
2-Phenyl-8-trifluoromethyl-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 of the synthesis of 4a, using 3h and phenyl hydrazine. 1H NMR (DMSO-d6) δ (ppm):7.21 (1H, m), 7.42 (2H, t, J=7.56 Hz), 7.97 (1H, d, J=2.20 Hz), 8.00 (1H, d, J=2.20 Hz), 8.20 (1H, ddd, J=7.41, 1.10, 0.83 Hz), 8.43 (2H, dd, J=1.33, 0.83 Hz), 8.82 (1H, s). m/z 330.2 (MH+).

来源

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