64096-87-3Relevant academic research and scientific papers
NEW PROCESS FOR THE PREPARATION OF AMENAMEVIR
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Page/Page column 6-7, (2020/12/30)
The present invention relates to an improved process for the preparation of Amenamevir and derivatives thereof via a four component Ugi reaction.
METHOD FOR PRODUCING 1,1-DIOXO-HEXAHYDRO-THIOPYRAN-4-CARBOXYLIC ACID OR DERIVATIVE THEREOF
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Paragraph 0069; 0075, (2018/06/05)
PROBLEM TO BE SOLVED: To provide a practical and efficient method for producing 1,1-dioxo-hexahydro-thiopyran-4-carboxylic acid or a derivative thereof in an industrial scale. SOLUTION: Provided ia a method for producing 1,1-dioxo-hexahydro-thiopyran-4-carboxylic acid represented by the following formula or a derivative thereof, comprising: (step 1) a step of mesylating two hydroxy groups of di(2-hydroxyethyl) sulfone; (step 2) a step of condensing the dimesylated body with meldrum acid to obtain 3,3-dimethyl-9,9-dioxo-2,4-dioxa-9-thiaspiro[5.5]undecane-1,5-dione; and (step 3) a step of hydrolyzing and decarbonating the aforementioned compound to obtain 1,1-dioxo-hexahydro-thiopyran-4-carboxylic acid. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT
Compounds Which Modulate The CB2 Receptor
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Page/Page column 74, (2010/02/17)
Compounds of formula (I) are disclosed. Compounds according to the and are useful for treating inflammation. Those compounds which are agonists are additionally useful for treating pain.
HETEROCYCLIC COMPOUNDS WHICH MODULATE THE CB2 RECEPTOR
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Page/Page column 120, (2010/09/17)
Compounds which modulate the CB2 receptor are disclosed. Compounds according to the invention bind to and are agonists of the CB2 receptor, and are useful for treating inflammation. Those compounds which are agonists are additionally useful for treating pain.
A practical, efficient synthesis of 1,1-dioxo-hexahydro-1#-thiopyran-4- carbaldehyde
Bio, Matthew M.,Hansen, Karl B.,Gipson, John
, p. 892 - 895 (2013/01/03)
A practical, efficient, and scalable procedure for the preparation of l,1-dioxo-hexahydro-1λ6-thiopyran-4-carbaldehyde is reported. Synthesis of this aldehyde was complicated by high aqueous solubility of the product and the intermediates. The isolation and purification of the aldehyde was accomplished by conversion to the crystalline bisulfite adduct.
TRIAZOLYLPIPERIDINE DERIVATIVES AND USE THEREOF IN THERAPY
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, (2010/11/25)
The present invention provides compounds of formula (I) Wherein R1 , R2, R3 , R4 , Het and m are as defined in the description. The compounds of the present invention are modulators, especially antagonists, of the activity of chemokine CCR5 receptors.
FUSED HETEROCYCLIC COMPOUNDS
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Page 56, (2010/02/07)
Compounds, compositions and methods are provided that are useful in the treatment and/or prevention of a condition or disorder mediated by a G-protein coupled receptor. In particular, the compounds of the invention are useful in the treatment and/or prevention of eating disorders, obesity, anxiety disorders and mood disorders.
