60703-46-0Relevant academic research and scientific papers
HETEROCYCLIC COMPOUNDS AND METHODS OF USE THEREOF
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Paragraph 0199, (2021/12/28)
The present disclosure relates to inhibitors of one or more isoforms of RAS, such as inhibitors of one or more of KRAS, HRAS and NRAS, or mutants thereof, such as G12D, G12V, G13D or G12C mutants thereof. Therapeutic methods of treating conditions and dis
Synthesis method of 2,4,6,-trichloro-5-methoxypyrimidine
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Paragraph 0014-0017, (2019/10/15)
The invention discloses a synthesis method of 2,4,6,-trichloro-5-methoxypyrimidine, the synthesis method comprises the following steps of: 1, mixing 2,4,6-trihydroxy-5-methoxypyrimidine, phosphorus oxychloride and an organic base according to a weight ratio of 1: 5-10: 0.33-0.7, and performing chlorination reaction at 25-100 DEG C for 2-5 hours; and 2, after the reaction is completed, cooling a mixture, concentrating the mixture under a reduced pressure to remove excess phosphorus oxychloride, quenching with water, extracting with an organic solvent, drying, and concentrating to obtain a product. The method not only improves the yield, shortens the time, is simple to operate, simplifies the post-treatment process, saves the cost, and is suitable for popularization.
DIOXINO-AND OXAZIN-[2,3-D]PYRIMIDINE PI3K INHIBITOR COMPOUNDS AND METHODS OF USE
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Page/Page column 0175, (2014/03/25)
Dioxino-and oxazin-[2,3-d]pyrimidine PI3K inhibitor compounds of Formula I with anti-cancer activity, anti-in-flammatory activity, or immunoregulatory properties, and more specifically with PI3 kinase modulating or inhibitory activity are de-scribed. Methods are described for using the tricyclic PI3K inhibitor compounds of Formula I for in vitro, in situ, and in vivo diagnosis or treatment of mammalian cells, organisms, or associated pathological conditions.
TRICYCLIC PI3K INHIBITOR COMPOUNDS AND METHODS OF USE
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Page/Page column 84, (2012/06/30)
Tricyclic PI3k inhibitor compounds of Formula I with anti-cancer activity, anti- inflammatory activity, or immunoregulatory properties, and more specifically with PI3 kinase modulating or inhibitory activity are described. Methods are described for using the tricyclic PI3K inhibitor compounds of Formula I for in vitro, in situ, and in vivo diagnosis or treatment of mammalian cells, organisms, or associated pathological conditions. Formula I compounds include stereoisomers, geometric isomers, tautomers, and pharmaceutically acceptable salts thereof. The dashed lines indicate an optional double bond, and at least one dashed line is a double bond. The substituents are as described.
NOVEL PYRIMIDINE COMPOUNDS AS MTOR AND P13K INHIBITORS
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Page/Page column 217-218, (2011/07/30)
The present invention relates to pyrimidine compounds of formula (I): which are useful in treating mTOR kinase- or PI3K kinase-related diseases.
Pyrimidines
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, (2008/06/13)
Compounds having the formula SPC1 Process for the preparation of such compounds which comprises reacting a pound having the formula: SPC2 Medicaments containing a compound of formula (I) or a salt thereof with a pharmaceutically acceptable acid; compounds
