Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Pyridines, sulfonamido

To benzo[A]quinolinyl palladium(II) pyridine-sulfonamido complex (12.8 mg, 0.0200 mmol) in acetonitrile-c/i (0.6 mL) at 23 °C was added l-chloromethyl-4-fluoro-l,4-diazoniabicyclo [2.2.2]octane bis(tetrafluoroborate) (7.1 mg, 0.020 mmol). After stirring for 10 min at 23 °C, the colorless suspension formed a dark purple solution. The complex was characterized by nuclear magnetic resonance (NMR spectroscopy) in acetonitrile solution without purification. ... [Pg.789]

Into a solution of 15.9 grams of 3-amino-2-phenyl-pvrazole in 60 cc of anhydrous pyridine, 29 grams of p-carbethoxyamino-benzene sulfonyl chloride are introduced within about 25 minutes. When the reaction subsides, heating is carried out for a further hour to 90° to 95°C internal temperature. The reaction solution is then poured into 300 cc of 2 N hydrochloric acid. The precipitate is filtered with suction and recrystallized from dilute alcohol. The 3-(p-carbethoxyaminobenzene sulfonamido)-2-phenyl-pvrazole is obtained thus in white crystals of MP 175° to 176°C. [Pg.1419]

The 3-sulfonamido-4-(3-methylbenzyl)amino-pyridine crystallized in the form of beige coloured cristals having a melting point of 184°-186°C. [Pg.3294]

Carbinolamides (derived from keto amides) afford 2-sulfonamido-substituted furans when treated with Tf20 and pyridine (eq 61). ... [Pg.514]


See other pages where Pyridines, sulfonamido is mentioned: [Pg.789]    [Pg.789]    [Pg.95]    [Pg.1409]    [Pg.1412]    [Pg.1612]    [Pg.2442]    [Pg.243]    [Pg.266]    [Pg.830]    [Pg.830]    [Pg.830]    [Pg.3097]    [Pg.3099]    [Pg.3294]    [Pg.279]    [Pg.95]    [Pg.551]    [Pg.95]    [Pg.551]    [Pg.291]    [Pg.1409]    [Pg.1412]    [Pg.1419]    [Pg.240]   
See also in sourсe #XX -- [ Pg.422 , Pg.423 ]




SEARCH



© 2024 chempedia.info