Paper
SYNTHESIS OF 5-CHLORO-3-METHYL-1 PHENYL-1Η PYRAZOLE-4-CARBOXYLIC ACID HETEROCYCLIC-2-YLAMIDE
Published 2003 · H. Liming, Liu Xueshu, Chen Zhiyuan
Heterocyclic Communications
Q3 SJR score
2
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0
Influential Citations
Abstract
Reaction of 5-chloro-3-methyl-l-phenyl-lH-pyrazole-4-carbonyl chloride 4 with substituted benzothiazol-2-ylamine and substituted [1,3,4] thiadiazol-2-ylamine yields 5-chloro-3-methyl-l-phenyl-1Η pyrazole-4-carboxylic acid-substituted benzothiazol-2-ylamide 5 and 5-chloro-3-methyl-1-phenyl-1Η pyrazole4-carboxylic acid (5-substituted -[1,3,4] thiadiazol-2-yl)amide 6 respectively in good yields.
Study Snapshot
5-CHLORO-3-METHYL-1 PHENYL-1 PYRAZOLE-4-CARBOXYLIC ACID HETROCYCLIC-2-YLAMIDE CAN BE SUBSTATED BY SUBSTATED BENOXITAZOL-2-YLAM
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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