147992-87-8Relevant articles and documents
Synthesis method of thienopyridine medical intermediate
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Paragraph 0023; 0024; 0025, (2016/10/27)
The invention discloses a synthesis method of a thienopyridine medical intermediate. The method takes malononitrile as the raw material to prepare the product by six-step reaction. The thienopyridine medical intermediate involved in the invention is 3-amino-4-(dimethylamino)thieno[2, 3-b]pyridine carboxamide. The invention adopts two brand new synthetic methods for preparation of 3-amino-4-(dimethylamino)thieno[2, 3-b]pyridine carboxamide from 2-chloro-4-(dimethylamino)nicotinonitrile, the method is simple and easy to operate, and the atom economy is high.
THIENOPYRIDINE DERIVATIVES
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Page/Page column 63, (2010/11/26)
The present invention provides a compound promoting osteogenesis. The present invention provides a compound having the following general formula (I) wherein R 1 is H or alkyl, R 2 is R a S-, R a O-, R a NH-, R a (R b )N- or cyclic amino, and R a and R b are alkyl which may be substituted, cycloalkyl which may be substituted, or the like, or a pharmacologically acceptable salt thereof.
SYNTHESIS AND BIOLOGICAL PROPERTIES OF 4-PHENYLAMINO- AND 4-DIMETHYLAMINO-3-CYANOPYRIDINE-2-THIONES AND THE THIENOPYRIDINES OBTAINED FROM THEM
Kadushkin, A. V.,Faermark, I. F.,Shvarts, G. Ya.,Granik, V. G.
, p. 870 - 874 (2007/10/02)
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