反应 #1885073

ord-8ed176e5daa64842ae9a0ff5a8253e0e

反应方程式

CCOC(=O)c1cnc2ccccc2c1Cl
ethyl 4-chloro-quinoline-3-carboxylate
CCOC(=O)c1cnc2ccccc2c1Cl
Ethyl 4-chloro-quinoline-3-carboxylate
CCN(CC)CC
triethylamine
NNc1ccccc1
phenyl hydrazine
O=c1c2c[nH]c3ccccc3c-2nn1-c1ccccc1
crude product
O=c1c2c[nH]c3ccccc3c-2nn1-c1ccccc1
2-Phenyl-2,5-dihydro-pyrazolo-(4,3-c) quinolin-3-one

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

A suspension of ethyl 4-chloro-quinoline-3-carboxylate (3a) (2.35 g, 0.01 M) in 20 mL of o-xylene was refluxed with triethylamine (2.0 mL, 0.02 M) and phenyl hydrazine (2.89 g, 0.02 M) overnight. The crude product was obtained by filtration followed by washing the solid with cold methanol.

来源

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