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A synthesis of highly substituted 2,4-diacylpyrroles through a Cu-catalyzed dimerization of acylazirines generated in situ by a photochemical valence isomerization is described. The shown methodology allows the use of simple precursors and a readily available copper(II)-catalyst. Since the reaction is best performed at elevated temperatures, a method to adjust the temperature of the reaction mixture during this dual light and metal-induced process was established. Additionally, mechanistic studies of the reaction were performed in order to provide a deeper understanding of the chemistry of 2-acylazirines.

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Isoxazole – Wikipedia,
Isoxazole | C3H3NO – PubChem

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The interaction of 4-cinnamylideneamino-3-methyl-5-styrylisoxazoles (1) with dimethyl acetylenedicarboxylate has given an isoxazolyldihydropyridine (2) as major and an isoxazolylaminofumarate (3) as minor products respectively. 3-Cinnamylideneamino-5-methylisoxazoles (4) behave similarly.Isoxazolylaminofumarates (3 and 6) have been identified by unambiguous synthesis.

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This invention describes a process for the preparation of N-(4-trifluoromethyl)-5-methylisoxazole-4-carboxamide commonly known as leflunomide comprising : (a) reacting ethylaceto acetate, triethylorthoformate, and acetic anhydride with simultaneous distillation to form ethyl ethoxymethyleneacetoacetic ester; (b) reacting the ethyl ethoxymethyleneacetoacetic ester with aqueous hydroxylamine without using any external base and without any distillation to form ethyl-5-methylisoxazole-4-carboxylate; (c) reacting the ethyl-5-methylisoxazole-4-carboxylate with strong acid to form -5-methylisoxazole-4-carboxylic acid; (d) 5-methylisoxazole-4-carboxylic acid is reacted with thionyl chloride in presence of N, N-Dimethylformamide and equimolar of 4-trifluoromethylaniline without any external base to obtain highly pure Leflunomide.

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Compounds of formula (I) and formula (II) are disclosed. Compounds according to the invention bind to and are agonists, antagonists or inverse agonists of the CB2 receptor, and are useful for treating inflammation. Those compounds which are agonists are additionally useful for treating pain

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More research is needed about 5-(4-Hydroxyphenyl)isoxazole-3-carboxylic acid

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In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 33282-15-4, name is 5-(4-Hydroxyphenyl)isoxazole-3-carboxylic acid, introducing its new discovery. Product Details of 33282-15-4

An iridium complex successfully catalyzed the annulation of various N-arylcarbamoyl chlorides with internal alkynes to afford 2-quinolones in good to excellent yields. The present reaction is widely applicable to substrates with various functionalities. An amide-iridacycle complex was isolated, and it is likely that such an iridacycle species is a key intermediate in the catalytic reaction.

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The linear product is formed as the major product when in situ generated titanium complexes with aminopyridinato ligands are used as catalysts for hydroaminoalkylation reactions of styrenes (see scheme). The reaction is not limited to the use of N-methylanilines and for the first time can be performed with N-alkylanilines bearing alkyl groups larger than methyl, or even with dialkylamines. The best selectivities in favor of a linear product are better than 90:10. Copyright

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Reference of 3209-70-9, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.3209-70-9, Name is Ethyl isoxazole-3-carboxylate, molecular formula is C6H7NO3. In a Patent,once mentioned of 3209-70-9

3-Substituted pyrrolidines having a 4-carboxypiperidinylmethyl substituent on the 4-position of the ring are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptors CCR-3 and/or CCR-5.

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Some scientific research about 3,5-Dimethylisoxazole

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In heterogeneous catalysis, the catalyst is in a different phase from the reactants. Safety of 3,5-Dimethylisoxazole, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 300-87-8, name is 3,5-Dimethylisoxazole. In an article,Which mentioned a new discovery about 300-87-8

Reaction of isoxazoles in the presence of Mo(CO)6 and water causes reductive cleavage of the N-O bond to give beta-aminoenones in good yields.

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A quinolone derivative represented by general formula (1) or a salt thereof, and an antibacterial containing the same, wherein R¹ represents isoxazolyl or isothiazolyl each of which may be substituted; R² represents hydrogen, halogen, lower alkyl, hydroxy, amino or nitro; R³ represents hydrogen or halogen; and Y represents halogen, optionally substituted saturated cyclic amino or H2N-(CH2)m-A-. This compound is useful as an antibacterial, can be used as medicines for humans and animals, drugs for fishes, pesticides and food preservative, and is expected to have an anti-HIV activity.

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Isoxazole – Wikipedia,
Isoxazole | C3H3NO – PubChem

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FMS-like Tyrosine Kinase 3 (FLT3) is a clinically validated target for acute myeloid leukemia (AML). Inhibitors targeting FLT3 have been evaluated in clinical studies and have exhibited potential to treat FLT3-driven AML. A frequent, clinical limitation is FLT3 selectivity, as concomitant inhibition of FLT3 and c-KIT is thought to cause dose-limiting myelosuppression. Through a rational design approach, novel FLT3 inhibitors were synthesized employing a pyridine/pyrimidine warhead. The most potent compound identified from the studies is compound 13a, which exhibited an IC50 value of 13.9 ± 6.5 nM against the FLT3 kinase with high selectivity over c-KIT. Mechanism of action studies suggested that 13a is a Type-II kinase inhibitor, which was also supported through computer aided drug discovery (CADD) efforts. Cell-based assays identified that 13a was potent on a variety of FLT3-driven cell lines with clinical relevance. We report herein the discovery and therapeutic evaluation of 4,6-diamino pyrimidine-based Type-II FLT3 inhibitors, which can serve as a FLT3-selective scaffold for further clinical development.

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Reference:
Isoxazole – Wikipedia,
Isoxazole | C3H3NO – PubChem