116344-32-2Relevant articles and documents
CALPAIN MODULATORS AND THERAPEUTIC USES THEREOF
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, (2018/04/17)
Disclosed herein are small molecule calpain modulator compositions, pharmaceutical compositions, the use and preparation thereof.
New reactivity of nitropyrimidinone: Ring transformation and N-C transfer reactions
Nishiwaki, Nagatoshi,Matsushima, Kazuo,Chatani, Miki,Tamura, Mina,Ariga, Masahiro
, p. 703 - 707 (2007/10/03)
Nitropyrimidinone 1 revealed new reactivity upon treatment with active methylene compounds 2 under basic conditions. The N1-C2-C3-C4 moiety of 1 combined with two carbon units of 2 affording polyfunctionalized pyridones 4, which was hitherto unknown ring transformation. On the other hand, the N1-C2 moiety of 1 was transferred to the methylene group of 2 giving functionalized enamines 3. It was also possible to modify the amino group in 3a by reactions with primary amines. Enamines 3 reacted with hydrazines, and leading to functionalized pyrazoles 7 quantitatively. The ratios of regioisomeric pyrazoles 7/8 were moderately controlled by use of sterically hindered enamines 3h, 3k and 31. Furthermore, enamine 3a was readily converted to 1,4-diazepines 9 having a functional group at the 6-position.
A CONVENIENT SYNTHESIS OF 2-PYRAZOLINES AND PYRAZOLES FROM ALDEHYDE HYDRAZONES AND ETHYL PROPIOLATE
Kamitori, Yasuhiro,Hojo, Masaru,Masuda, Ryoichi,Fujishiro, Masaki,Wada, Masaaki
, p. 21 - 26 (2007/10/02)
Aldehyde methylhydrazones (3) reacted with ethyl propiolate in the presence of acetic acid affording 4-ethoxycarbonyl-1-methyl-2-pyrazolines (4) in 13-44percent yields.Easily 4 was dehydrated to the corresponding pyrazoles (6) by treatment with H2O2 in the presence of FeCl2.