Category: isoxazole

Arora, Komal published the artcileSynthesis, configurational analysis and antimicrobial activity of imidazolidinone, thiazolidinone and isoxazolone derivatives of 9,10-phenanthrenequinone, Category: isoxazole, the publication is Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry (2011), 50B(1), 83-88, database is CAplus.

Knoevenagel-type condensations of phenanthrenequinone with imidazolidinones, thiazolidinones, and isoxazolone were described. The newly synthesized products were characterized by spectral data. The exclusive formation of anti-configuration of the mono-condensation product was explained on the basis of AM1 calculations Some of the products were screened for antimicrobial activity.

Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry published new progress about 1076-59-1. 1076-59-1 belongs to isoxazole, auxiliary class Oxazoline,Benzene,Ester, name is 3-Phenylisoxazol-5(2H)-one, and the molecular formula is C9H7NO2, Category: isoxazole.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Terent’ev, Alexander O. published the artcileSelective Oxidative Coupling of 3H-Pyrazol-3-ones, Isoxazol-5(2H)-ones, Pyrazolidine-3,5-diones, and Barbituric Acids with Malonyl Peroxides: An Effective C-O Functionalization, Application of 3-Phenylisoxazol-5(2H)-one, the publication is ChemistrySelect (2017), 2(11), 3334-3341, database is CAplus.

Oxidative functionalization of 3H-pyrazol-3-ones, isoxazol-5(2H)-ones, pyrazolidine-3,5-diones, and barbituric acids by malonyl peroxides results exclusively in C-O coupling products. Traditional hydroxylation, formation of carbonyl groups, or oxidative destruction of the heterocyclic ring are not observed Under optimized reactions conditions – fluorinated alcs. as activating medium and at room temperature (20 – 25°) – the selective C-O coupling proceeds in high yields (up to 94 %). The oxidative insertion into the enolizable C-H bond of the substrate is mechanistically viewed as a nucleophilic attack by the heterocycle onto the electrophilically activated malonyl peroxides. For heterocyclic substrates with an active methylene group – 3H-pyrazol-3-ones, isoxazol-5(2H)-ones, and barbituric acids – both C-H bonds are oxidized to afford double oxidative C-O coupling products in good yields (up to 72 %).

ChemistrySelect published new progress about 1076-59-1. 1076-59-1 belongs to isoxazole, auxiliary class Oxazoline,Benzene,Ester, name is 3-Phenylisoxazol-5(2H)-one, and the molecular formula is C9H9NO6S, Application of 3-Phenylisoxazol-5(2H)-one.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Toran, Ricardo published the artcileOrganocatalytic Enantioselective 1,6-aza-Michael Addition of Isoxazolin-5-ones to p-Quinone Methides, Quality Control of 1076-59-1, the publication is European Journal of Organic Chemistry (2020), 2020(5), 627-630, database is CAplus.

A thiourea-Bronsted base bifunctional catalyst allowed the enantioselective 1,6-aza-Michael addition of isoxazolin-5-ones to p-quinone methides to give isoxazolin-5-ones having a chiral diarylmethyl moiety attached to the N atom with fair to good yields and enantiomeric excesses. To the best of our knowledge this reaction represents the first example of enantioselective N-alkylation of isoxazolin-5-ones as well as the first example of enantioselective 1,6-aza-Michael reaction involving p-quinone methides.

European Journal of Organic Chemistry published new progress about 1076-59-1. 1076-59-1 belongs to isoxazole, auxiliary class Oxazoline,Benzene,Ester, name is 3-Phenylisoxazol-5(2H)-one, and the molecular formula is C20H40O2, Quality Control of 1076-59-1.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Chacon Simon, Selena published the artcileDiscovery of WD Repeat-Containing Protein 5 (WDR5)-MYC Inhibitors Using Fragment-Based Methods and Structure-Based Design, COA of Formula: C8H5F3N4, the publication is Journal of Medicinal Chemistry (2020), 63(8), 4315-4333, database is CAplus and MEDLINE.

The frequent deregulation of MYC and its elevated expression via multiple mechanisms drives cells to a tumorigenic state. Indeed, MYC is overexpressed in up to ~50% of human cancers and is considered a highly validated anticancer target. Recently, we discovered that WD repeat-containing protein 5 (WDR5) binds to MYC and is a critical cofactor required for the recruitment of MYC to its target genes and reported the first small mol. inhibitors of the WDR5-MYC interaction using structure-based design. These compounds display high binding affinity, but have poor physicochem. properties and are hence not suitable for in vivo studies. Herein, we conducted an NMR-based fragment screening to identify addnl. chem. matter and, using a structure-based approach, we merged a fragment hit with the previously reported sulfonamide series. Compounds in this series can disrupt the WDR5-MYC interaction in cells, and as a consequence, we observed a reduction of MYC localization to chromatin.

Journal of Medicinal Chemistry published new progress about 2251-79-8. 2251-79-8 belongs to isoxazole, auxiliary class Trifluoromethyl,Fluoride,Benzene, name is 5-(4-(Trifluoromethyl)phenyl)-1H-tetrazole, and the molecular formula is C8H5F3N4, COA of Formula: C8H5F3N4.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Feng, Dapeng published the artcileEffects of parecoxib sodium on prevention of emergence agitation during the recovery period of general anesthesia for the patients undergoing epigastric surgeries, Formula: C19H17N2NaO4S, the publication is Guoji Mazuixue Yu Fusu Zazhi (2014), 35(7), 613-616, database is CAplus.

The objective of this paper was to observe the preventive effects of parecoxib sodium on occurrence of emergence agitation during the recovery period of general anesthesia for the patients who underwent epigastric surgeries. One hundred and twenty patients, ASA I∼II, undergoing elective epigastric surgeries were divided randomly into four groups, with 30 cases in each group. Anesthesia of all patients was maintained with sevoflurane and remifentanil, keeping the bispectral index (BIS) around 40-50. Parecoxib sodium 0.8 mg/kg was i.v. infused into the patients just before anesthesia induction in group A and just before the closure of peritoneum in group B, sufentanil 0.08μg/kg was injected just before the closure of peritoneum in group C, and 2 mL saline as placebo was administrated in group D. The level of agitation(RS), visual analog scales(VAS) and ramsay sedation score(RSS) were evaluated during the recovery period of general anesthesia. Mean arterial pressure(MAP) and heart rate(HR) were monitored at preinduction (T1), 10 min before tracheal extubation (T2), immediately after tracheal extubation (T3) and 10 min after tracheal extubation (T4). The recovery times of group A, B, D(7±3), (8±4), (7±3) min were significantly shorter than those of group C. Requirement of remifentanil in group A (0.8±0.3) mg was significantly lower than that of group D (1.3±0.5) mg (P<0.05). At T3, the MAP and HR in group D(126±25) mmHg(1 mmHg=0.133 kPa) (106±28) beats/min were significantly higher than those in group A[(106±25) mmHg, (96±25) beats/min], group B [(113±27) mmHg, (99±27) beats/min], group C [(111±27) mmHg, (86±19) beats/min](P<0.05), which happened similarly at T4. Compared with group D, the incidence of agitation (33.3%) was significantly higher than that of group A (6.7%), group B (13.2%) and group C (10.0%) (P<0.05), and the incidence of agitation group A was significantly lower than group B (P<0.05). Compared with group D, the median of score of VAS was 5, which was significantly higher than that of group A (2), group B (3), and group C (2) (P<0.05). Compared with group D, the median of score of RSS was 4, which was significantly higher than that of group A (3), group B (3) and group C (3) resp. (P<0.05). The incidence of nausea and vomiting of group C was much higher than other groups significantly (P<0.05). Parecoxib sodium had analgesic effect for the patients of epigastric surgeries, preventing the incidence of postoperative agitation and adverse reactions during the recovery period of general anesthesia.

Guoji Mazuixue Yu Fusu Zazhi published new progress about 198470-85-8. 198470-85-8 belongs to isoxazole, auxiliary class Immunology/Inflammation,COX, name is Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, and the molecular formula is C19H17N2NaO4S, Formula: C19H17N2NaO4S.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Cao, Jing published the artcileOrganocatalytic Oxidative Amidation of Aldehydes with Tetrazoles to Construct 2,5-Diaryl 1,3,4-Oxadiazoles, Recommanded Product: 5-(4-(Trifluoromethyl)phenyl)-1H-tetrazole, the publication is Chinese Journal of Chemistry (2015), 33(11), 1239-1243, database is CAplus.

A practical and metal-free oxidative amidation of aldehydes with tetrazoles into 1,3,4-oxadiazoles was developed by employing tetrabutylammonium iodide (TBAI) as catalyst and tert-Bu hydroperoxide (TBHP) as oxidant. A wide range of 2,5-disubstituted 1,3,4-oxadiazoles was conveniently generated in moderate to good yields. Gram-scale reaction was also realized in this catalytic system.

Chinese Journal of Chemistry published new progress about 2251-79-8. 2251-79-8 belongs to isoxazole, auxiliary class Trifluoromethyl,Fluoride,Benzene, name is 5-(4-(Trifluoromethyl)phenyl)-1H-tetrazole, and the molecular formula is C8H5F3N4, Recommanded Product: 5-(4-(Trifluoromethyl)phenyl)-1H-tetrazole.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Li, Zhengyi published the artcilePalladium-Catalyzed Aminocarbonylation Reaction to Access 1,3,4-Oxadiazoles using Chloroform as the Carbon Monoxide Source, Computed Properties of 2251-79-8, the publication is Advanced Synthesis & Catalysis (2015), 357(16-17), 3469-3473, database is CAplus.

A palladium-catalyzed aminocarbonylation reaction of aryl halides with chloroform and tetrazoles has been developed, where chloroform was employed as the carbon monoxide (CO) source in the presence of cesium hydroxide. The in situ generated N-acylated tetrazoles were unstable and easily decomposed to afford 2,5-disubstituted 1,3,4-oxadiazoles. A wide range of tetrazoles and aryl halides reacted smoothly under the optimized reaction conditions to give the corresponding products in moderate to good yields.

Advanced Synthesis & Catalysis published new progress about 2251-79-8. 2251-79-8 belongs to isoxazole, auxiliary class Trifluoromethyl,Fluoride,Benzene, name is 5-(4-(Trifluoromethyl)phenyl)-1H-tetrazole, and the molecular formula is C8H5F3N4, Computed Properties of 2251-79-8.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Zhu, Kai-qiang published the artcileIron-catalyzed oxidative dehydrogenative coupling of ethers with aryl tetrazoles, Category: isoxazole, the publication is Tetrahedron Letters (2015), 56(34), 4943-4946, database is CAplus.

An iron-catalyzed oxidative dehydrogenative coupling of ethers with aryl tetrazoles has been developed. A wide variety of tetrazoles and ethers survived the reaction conditions to deliver the corresponding hemiaminal derivatives in moderate to good yields.

Tetrahedron Letters published new progress about 2251-79-8. 2251-79-8 belongs to isoxazole, auxiliary class Trifluoromethyl,Fluoride,Benzene, name is 5-(4-(Trifluoromethyl)phenyl)-1H-tetrazole, and the molecular formula is C7H4BrClO2, Category: isoxazole.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Lobbecke, Stefan published the artcileThermoanalytical screening of nitrogen-rich substances, Formula: C8H5F3N4, the publication is Propellants, Explosives, Pyrotechnics (1999), 24(3), 168-175, database is CAplus.

The thermal decomposition behavior of ∼60 nitrogen-rich tetrazole-class and tetrazine-class compounds was investigated by thermoanal. methods. The decomposition mechanisms initiated by ring opening of the heterocycles could be established. Substituent effects on the exothermic decomposition characteristics of nitrogen-rich compounds were demonstrated.

Propellants, Explosives, Pyrotechnics published new progress about 2251-79-8. 2251-79-8 belongs to isoxazole, auxiliary class Trifluoromethyl,Fluoride,Benzene, name is 5-(4-(Trifluoromethyl)phenyl)-1H-tetrazole, and the molecular formula is C8H5F3N4, Formula: C8H5F3N4.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Wan, Ting published the artcileRh(III)-Catalyzed [4 + 2] Annulation of 3-Aryl-5-isoxazolone with Maleimides or Maleic Ester, Synthetic Route of 1076-59-1, the publication is Organic Letters (2020), 22(16), 6484-6488, database is CAplus and MEDLINE.

The Rh(III)-catalyzed [4 + 2] annulation of 3-aryl-5-isoxazolones with maleimides or maleic ester has been developed, which gives synthetically important 3,4-dihydroisoquinoline derivatives in good to excellent yields. This facile protocol can tolerate a variety of functional groups, and CO₂ was produced as the predominant byproduct. Notably, a C-C bond and a C-N bond were formed simultaneously. This protocol could be easily scaled up.

Organic Letters published new progress about 1076-59-1. 1076-59-1 belongs to isoxazole, auxiliary class Oxazoline,Benzene,Ester, name is 3-Phenylisoxazol-5(2H)-one, and the molecular formula is C15H14Cl2S2, Synthetic Route of 1076-59-1.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem