50998-05-5Relevant academic research and scientific papers
THIADIAZOLE-SUBSTITUTED ARYLAMIDES AS P2X3 AND P2X2/3 ANTAGONISTS
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Page/Page column 19, (2010/06/22)
Compounds of the formula I: or a pharmaceutically acceptable salt thereof, wherein, R1 is optionally substituted thiadiazolyl, and R2, R3, R4, R5, R6, R7 and R8 are as defined herein. Also disclosed are methods of using the compounds for treating diseases associated with P2X3 and/or a P2X2/3 receptor antagonists and methods of making the compounds.
PYRIMIDINES WITH TIE2 (TEK) ACTIVITY
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Page/Page column 135, (2010/02/12)
The invention relates to a compound of the Formula (I). or salt thereof wherein R1, R2, R3, R4, R5, R6, A, B, L, n and m are as defined in the description. The invention also relates to pharmaceutical compositions of said compounds, the use of said compounds as medicaments and in the production of an anti-angiogenic effect in a warm-blooded animal. The invention also relates to processes for the preparation of said compounds.
Nosylaziridines: Activated aziridine electrophiles
Maligres, Peter E.,See, Marjorie M.,Askin, David,Reider, Paul J.
, p. 5253 - 5256 (2007/10/03)
Nosylaziridines are highly reactive electrophiles towards a variety of nucleophiles yielding the corresponding SN2 adducts without competing attack on the nosyl functionality (SNAr). The resulting primary nosylamide adducts can he readily cleaved under mild conditions to provide the primary amines.
DIRECT NUCLEOPHILIC SUBSTITUTION IN 2-HALOALKYLAMINES: NEW ROUTE TO SUBSTITUTED ETHYLENEDIAMINES
Chechik, V. O.,Bobylev, V. A.
, p. 1501 - 1502 (2007/10/03)
Nucleophilic substitution in 2-haloalkylamines in weakly polar media was found to proceed partially without intermediate formation of aziridines.This makes it possible to obtain pure substituted ethylenediamines.
