78441-69-7Relevant articles and documents
Clean preparation method of 4-hydroxymethylthiazole and its intermediate
-
Paragraph 0082-0083, (2019/04/06)
The invention discloses a clean preparation method of 4-hydroxymethylthiazole and its intermediate. The clean preparation method includes, taking compound I as an example, the steps of in a solvent, subjecting compound IV and an alkali metal hypohalite to
HYDRAZONE DERIVATIVE
-
Page/Page column 47-48, (2010/11/08)
A compound represented by the following formula (I): wherein R1 represents hydrogen, aryl which may have a substituent, a saturated or unsaturated 5- to 7-membered heterocyclic group which may have a substituent, etc.; R2 represents hydrogen, aryl which may have a substituent, a saturated or unsaturated 5- to 7-membered heterocyclic group which may have a substituent, etc.; R3 represents hydrogen, etc.; Ar represents a divalent group derived from aromatic hydrocarbon, etc.; X represents a single bond, linear or branched alkylene having from 1 to 3 carbon atoms which may have a substituent, etc.; and G represents halogen, a saturated or unsaturated 5- or 6-membered cyclic hydrocarbon group which may have a substituent, a saturated or unsaturated 5- to 7-membered heterocyclic group which may have a substituent, etc., a salt thereof or a solvate thereof; and an agent for inhibiting aggregation and/or deposition of an amyloid protein or an amyloid-like protein, which comprises the compound, a salt thereof or a solvate thereof
2,3 Disubstituted- (5,6)-heteroarylfused-pyrimidine-4-ones
-
, (2008/06/13)
The present invention relates to novel compounds of the formula I, described above, and their pharmaceutically acceptable salts, and pharmaceutical compositions and methods of treating neurodegenerative and CNS-trauma related conditions.