反応 #62923

ord-54f00010d73a4fe7ad0b47e6da20449b

反応方程式

O=Cc1ccccc1
benzaldehyde
O=Cc1ccc(O)cc1
4-hydroxybenzaldehyde
NC1CCN(c2cc3c(cc2F)c(=O)c(C(=O)O)cn3-c2ccc(F)cc2)C1
acid ( 1 )
NC1CCN(c2cc3c(cc2F)c(=O)c(C(=O)O)cn3-c2ccc(F)cc2)C1
1-p-fluorophenyl-6-fluoro-1,4-dihydro-4-oxo-7-(3-amino-1-pyrrolidinyl)-quinoline-3-carboxylic acid
COc1ccc(C=NC2CCN(c3cc4c(cc3F)c(=O)c(C(=O)O)cn4-c3ccc(F)cc3)C2)cc1
1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(3-(4-hydroxybenzylidene)amino-1-pyrrolidinyl)-quinoline-3-carboxylic acid
COc1ccc(C=NC2CCN(c3cc4c(cc3F)c(=O)c(C(=O)O)cn4-c3ccc(F)cc3)C2)cc1
1-p-fluorophenyl-6-fluoro-1,4-dihydro-4-oxo-7-(3-(4-methoxybenzylidene)amino-1-pyrrolidinyl)-quinoline-3-carboxylic acid

反応条件

詳細条件
See reaction.notes.procedure_details.

実験手順

In the described fashion of Example 1 replacing benzaldehyde with 4-hydroxybenzaldehyde and using the acid (1) (R=cyclopropyl) described in Example 19 one obtains 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(3-(4-hydroxybenzylidene)amino-1-pyrrolidinyl)-quinoline-3-carboxylic acid (3) (R=cyclopropyl, Z=p-hydroxyphenyl); m.p. 273°-275° C.; Mass Spectrum, M/Z 435. Analytical Calculation for C24H22FN3O4.1/2H2O: C, 66.21; H, 5.06; N, 9.65. Found: C, 64.83; H, 5.01; N, 9.13.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04762845uspto-grants-1988_08