207922-56-3Relevant academic research and scientific papers
Tandem Condensation/Rearrangement Reaction of 2-Aminohetarene N-Oxides for the Synthesis of Hetaryl Carbamates
Bystrov, Dmitry M.,Zhilin, Egor S.,Fershtat, Leonid L.,Romanova, Anna A.,Ananyev, Ivan V.,Makhova, Nina N.
, p. 3157 - 3163 (2018/08/24)
A new approach to hetaryl carbamates through a tandem condensation/rearrangement reaction of 2-aminohetarene N-oxides was developed. The developed reaction is suitable for both five- and six-membered heterocycles and proceeds through the condensation of 2
Chloroformate free, scalable approach for the synthesis of organic carbamates and their alkylation
Shewalkar, Mukesh P.,Rao, Ramakrishna R.,Reddy, Veerbhadra,Darandale, Sunil N.,Shinde, Devanand B.
, p. 60 - 64 (2013/07/26)
A convenient method for the synthesis of organic carbamates of 2-aminopyridine without using hazardous chloroformate reagent is developed. This alternate approach for the synthesis of organic carbamates and their alkylation to 2-alkylaminopyridines is more practical and economical to be used on large scale. The amazing behavior of 2- aminopyridine helps in forming organic carbamates unlike 3-aminopyridine and 4-aminopyridine.
Process for substituted pyridines
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, (2008/06/13)
This invention relates to processes for preparing compounds of the formula (I) and to processes for preparing certain intermediates of the formula wherein R1is nitro, amino or protected amino; R2is H, fluoro, chloro CF3, n
BETA-ADRENERGIC AGONISTS TO REDUCE A WASTING CONDITION
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, (2008/06/13)
The present invention relates to the use of certain β-adrenergic agonists to reduce a wasting condition in a mammal (e.g., human).
Beta-Adrenergic agonists to reduce a wasting condition
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, (2008/06/13)
The present invention relates to the use of certain β-adrenergic agonists, their pharmaceutically acceptable prodrugs, pharmaceutically acceptable salts of either entity, or pharmaceutical compositions containing any of the foregoing, for the manufacture
