Reaction #336859

ord-d1d780ae30f24fec9ae1d8c93ea47bf8

Reaction equation

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)c1cnc2cc(F)c(F)cc2c1Cl
3c
CCOC(=O)c1cnc2cc(F)c(F)cc2c1Cl
Ethyl 4-chloro-6,7-difluoro-quinoline-3-carboxylate
NNc1ccccc1
phenyl hydrazine
O=c1c2c[nH]c3cc(F)c(F)cc3c-2nn1-c1ccccc1
title compound
O=c1c2c[nH]c3cc(F)c(F)cc3c-2nn1-c1ccccc1
7,8-Difluoro-2-phenyl-2,5-dihydro-pyrazolo-(4,3-c)quinolin-3-one

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Procedure

The title compound was prepared following the procedure described in Step 3 for the synthesis of 4a, using 3c and phenyl hydrazine. 1H NMR (DMSO-d6) δ (ppm): 7.18 (1H, t, J=7.82 Hz), 7.43 (2H, dd, J=8.30, 7.33 Hz), 7.75 (1H, dd, J=11.22, 7.32 Hz), 8.18, 3H, m), 8.90 (1H, s). m/z 298.2 (MH+).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07863266B2uspto-grants-2011_01