ChemInform Abstract: REACTION OF TERTIARY ARSINE SULFIDES WITH ACETYL CHLORIDE

1977 ◽  
Vol 8 (17) ◽  
pp. no-no
Author(s):  
B. E. ABALONIN ◽  
YU. F. GATILOV ◽  
G. I. VASILENKO
Author(s):  
A. S. Balueva ◽  
O. A. Erastov ◽  
T. A. Zyablikova
Keyword(s):  

2004 ◽  
Vol 1 (2) ◽  
pp. 93-98 ◽  
Author(s):  
H. S. Patel ◽  
H. D. Desai ◽  
H. J. Mistry

NovelN-substituted piperazine derivatives containing sulfonyloxy aniline moiety have been prepared. The various 4-sulfonyloxy aniline (SA) derivatives (2a-h) have been prepared by the condensation reaction ofN-Acetyl Sulfanilyl chloride (ASC) and sodium phenates followed by hydrolysis. The SA derivatives are then reacted with chloro acetyl chloride to give corresponding (N-Chloroacetyl) derivatives (3a-h). These derivatives are then reacted withN-phenyl piperazine to yield the corresponding piperazine derivatives (4a-h).


1982 ◽  
Vol 47 (6) ◽  
pp. 1005-1007 ◽  
Author(s):  
Boris Glavincevski ◽  
Sydney Brownstein

Author(s):  
Sha Li ◽  
Oskar Smaga ◽  
Yahan Sun ◽  
Xiaofang Li ◽  
Miłosz Pawlicki ◽  
...  

Acyl chlorides react with norcorrolatonickle(II) in dichloromethane in the presence of AlCl3 at room temperature affording two isomeric monoketone derivatives in moderate yields. For acetyl chloride, also diketones were detected...


INDIAN DRUGS ◽  
2017 ◽  
Vol 54 (11) ◽  
pp. 22-27
Author(s):  
A. Singh ◽  

A series of 4-(substituted aryl)- 1- [2’- methyl-6’- substituted anilino quinazolinon-4’-(3’H)-onyl ] -3- chloroazetidin- 2-ones 14-25 have been synthesized by addition of substituted anilines to 4-(substituted aryl)- 1- [2’- methyl-6’- bromoquinazolinon-4’-(3’H)-onyl ] -3- chloro- azetidin-2-ones 8-13 which in turn were prepared by the cycloaddition of triethylamine in dioxane to 3-(N-substituted benzylidene amino phenyl amido )-2-methyl-6-bromoquinazolin-4(3H)-ones 2-7 in presence of acetyl chloride. These compounds were screened for anticonvulsant activity and acute toxicity. Compound 4-(substituted aryl)- 1- [2’- methyl-6’- substituted anilino quinazolinon-4’-(3’H) – onyl ] -3- chloro-azetidinone showed most potent activity. The structure of all the synthesized compounds were delineated by elemental (C, H, N ) and spectra (IR, proton magnetic resonance and mass ) analysis.


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