反应 #1885075

ord-59d1bba5f774474e96bdc0e0b3b871a4

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
Cl.NNc1ccccc1F
2-fluorophenyl hydrazine hydrochloride
O=c1c2c[nH]c3ccccc3c-2nn1-c1ccccc1F
title compound
O=c1c2c[nH]c3ccccc3c-2nn1-c1ccccc1F
2-(2′-Fluorophenyl)-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 for the synthesis of 4a, using 2-fluorophenyl hydrazine hydrochloride instead of phenyl hydrazine hydrochloride. 1H NMR (DMSO-d6) δ (ppm): 7.13-7.46 (3H, m), 7.48-7.62 (2H, m), 7.67 (1H, dd, J=6.87, 1.37 Hz), 7.73 (1H, d, J=8.24 Hz), 8.11 (1H, dd, J=8.24, 1.09 Hz), 8.70 (1H, d, J=6.31 Hz). m/z 280.3 (MH+).

来源

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