Month: November 2022

On November 19, 2020, Allen, Bryce K.; Chamberlain, Brian T.; Dwight, Timothy A.; Huang, Huang; Kulkarni, Meghana M.; Lin, Zhixiong; Marino, Kristen A.; Niu, Deqiang; Shechter, Sharon; Swann, Steven published a patent.COA of Formula: C6H5BrN2O2 The title of the patent was Preparation of benzo[b][1,8]naphthyridine acetic acid derivatives as STING modulators useful in treatment and prevention of STING-associated diseases. And the patent contained the following:

The invention relates to preparation of benzonaphthyridine acetic acids(I) or pharmaceutically acceptable salts or esters thereof capable of binding to and modulating the activity of a stimulator of interferon genes (STING) protein. Compounds I wherein X is O, S, CH=CH, etc.; m is 1-3; Y is CN, OH, NH2, etc.; n is 1-4; Z is halo, CN, OH, etc.; etc., are claimed. The example compound II was prepared via multi-step synthesis using Me 2,6-dichloropyridine-3-carboxylic acid as starting material (procedure given). Compounds I were evaluated for their biol. activity (data given). Compounds I are effective modulators of STING, and can be used for the treatment and prevention of diseases caused by or associated with STING. The experimental process involved the reaction of 2-Amino-6-bromonicotinic acid(cas: 1196157-51-3).COA of Formula: C6H5BrN2O2

The Article related to benzonaphthyridine acetic acid preparation sting modulator disease treatment prophylaxis, Heterocyclic Compounds (More Than One Hetero Atom): Fused-Ring Systems With Two Or More Hetero Atoms, No More Than One Hetero Atom Per Ring and other aspects.COA of Formula: C6H5BrN2O2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

On January 3, 2013, Geneste, Herve; Ochse, Michael; Drescher, Karla; Behl, Berthold; Laplanche, Loic; Dinges, Juergen; Jakob, Clarissa published a patent.Product Details of 1214362-62-5 The title of the patent was Preparation of isoindole carboxamides, pyrrolopyridine carboxamides, and similar compounds as inhibitors of phosphodiesterase type 10A for treating neurological and psychiatric disorders. And the patent contained the following:

The present invention relates to novel carboxamide compounds of general formula I (wherein X1-X4 are N or (un)substituted CH, with provisos; A is O, S, SO, SO2, substituted N, or (un)substituted CH2; Het is monocyclic hetaryl, fused bicyclic hetaryl, or Ph, all of which may be substituted; and R7-R10 are independently H, halo, C1-4 alkyl, etc.), pharmaceutical compositions containing them, and their use in therapy. The compounds possess valuable therapeutic properties as inhibitors of phosphodiesterase type 10A and are particularly suitable for treating or controlling medical disorders selected from neurol. disorders and psychiatric disorders, for ameliorating the symptoms associated with such disorders and for reducing the risk of such disorders. Synthetic procedures for preparing I are exemplified. Example compound II was prepared in a 5-step synthesis that culminated in reaction of 4-methyl-[2,4′]bipyridinyl-3-carboxylic acid Me ester and 2-quinolin-2-ylethylamine. In a PDE10A inhibition assay, II had an IC50 <100 nM. The experimental process involved the reaction of Ethyl 2-bromo-6-fluorobenzoate(cas: 1214362-62-5).Product Details of 1214362-62-5

The Article related to isoindole pyrrolopyridine carboxamide preparation inhibitor pde10a neurol psychiatric disorder, Heterocyclic Compounds (More Than One Hetero Atom): Fused-Ring Systems With Two Or More Hetero Atoms, No More Than One Hetero Atom Per Ring and other aspects.Product Details of 1214362-62-5

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

On June 6, 2008, Kato, Shin-ichiro; Nonaka, Yasuhiro; Shimasaki, Toshiaki; Goto, Kenta; Shinmyozu, Teruo published an article.COA of Formula: C10H4Br2O8 The title of the article was Novel Pyromellitic Diimide-Based Macrocycle with a Linear π-Electronic System and Bis(phenylethynyl)pyromellitic Diimide: Syntheses, Structures, Photophysical Properties, and Redox Characteristics. And the article contained the following:

We report the syntheses, structures, photophys. properties, and redox characteristics of the [2+2] pyromellitic diimide-based macrocycle with a linear π-electronic system 2 as well as the 3,6-bis(phenylethynyl)pyromellitic diimide derivative 3. The interesting solid state structural properties of the clathrates of 3 with π-donors are also reported. The macrocycle 2 was synthesized by the direct cyclocondensation followed by the Sonogashira coupling reaction. X-ray crystallog. studies showed that the phenylacetylene moieties in 2 formed the intramol. benzene dimer structures, and the bis(phenylethynyl)pyromellitic diimide moieties in both 2 and 3 were stacked in a parallel and slanted arrangement. Theor. calculations for 2′ and 3 suggested the existence of electrostatic interactions between the bis(phenylethynyl)pyromellitic diimide moieties. The UV/vis spectral measurements and TDDFT calculations of 2, 2′, and/or 3 were performed to understand their electronic transitions. The fluorescence spectral measurements showed that 2 and 3 have visible fluorescence properties and 2 displays an excimer fluorescence at ca. 590 nm. The cyclic voltammetry measurements revealed that the electrostatic repulsion between the diimide moieties in 2 is greater than that in 1 according to the extension of the π-electronic systems. X-ray crystallog. of the clathrates of 3 with various π-donors demonstrated the formation of the segregated donor-acceptor structures, indicating the strong aggregation ability of the bis(phenylethynyl)pyromellitic diimide moiety. The experimental process involved the reaction of 3,6-Dibromobenzene-1,2,4,5-tetracarboxylic acid(cas: 41819-13-0).COA of Formula: C10H4Br2O8

The Article related to pyromellitic diimide based macrocycle preparation crystallog photophysics, Physical Organic Chemistry: Stereochemistry and Stereochemical Relationships, Including Conformational Inversions and Rotational Isomerization and other aspects.COA of Formula: C10H4Br2O8

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

On September 7, 2018, Stahl, Shannon S.; Gerken, James B.; Anson, Colin W.; Suh, Sung-Eun; Stamoulis, Alexiouis G. published a patent.Product Details of 41819-13-0 The title of the patent was Preparation of hydroquinones, anthraquinones and related compounds as high-and low-potential, water-soluble, robust quinones. And the patent contained the following:

Preparation of substituted hydroquinones, 1,4-quinones, catechols, 1,2-quinones, anthraquinones, and anthrahydroquinones od the exemplary formula I are disclosed herein. Compounds I wherein one or more of R1, R2, R3 and R4 include a sulfonate moiety, a sulfonimide moiety, or a phosphonate moiety, and any of R1, R2, R3 and R4 that do not include one of these moieties include an alkyl, a cycloalkyl, a thioether, a sulfoxide, a sulfone, a haloalkyl, a halogen, a nitrile, an imide, a pyrazole, or combinations thereof, are claimed. The substituted hydroquinones and catechols have the formula: while the substituted 1,4-quinones or 1,2-have the corresponding oxidized structure (1,4- benzoquinones and 1,2-benzoquinones). The substituted anthraquinones have the formula: while the substituted anthrahydroquinones have the corresponding reduced structure. Accordingly, they can be used as redox mediators in emerging technologies, such as in mediated fuel cells or organic-mediator flow batteries. The experimental process involved the reaction of 3,6-Dibromobenzene-1,2,4,5-tetracarboxylic acid(cas: 41819-13-0).Product Details of 41819-13-0

The Article related to hydroquinone anthraquinone preparation redox potential electrolyte fuel cell technol, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Phenols, Thiophenols, and Derivatives Including Phenol and Thiophenol Ethers and Esters and other aspects.Product Details of 41819-13-0

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

On May 20, 2022, Wu, Gaorong; Yang, Zhaoziyuan; Xu, Xiaobo; Hao, Liqiang; Chen, Lu; Wang, Yangyang; Ji, Yafei published an article.Related Products of 2567-29-5 The title of the article was Metal-Free Boron-Mediated ortho-C-H Hydroxylation of N-Benzyl-3,4,5-tribromopyrazoles. And the article contained the following:

A novel route was reported for C-H hydroxylation of benzyl compounds directed by a 3,4,5-tribromopyrazole auxiliary via boronation/oxidation using BBr3 and NaBO3·4H2O. The strategy exhibited outstanding site selectivity and afforded the corresponding phenols in moderate to excellent yields under metal-free conditions. Besides, this protocol was achieved in one pot, which is highly promising as a practical method for use in a multistep organic synthetic process. The experimental process involved the reaction of 4-(Bromomethyl)-1,1′-biphenyl(cas: 2567-29-5).Related Products of 2567-29-5

The Article related to benzyl tribromopyrazole preparation boron promoter regioselective hydroxylation, phenol preparation, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Phenols, Thiophenols, and Derivatives Including Phenol and Thiophenol Ethers and Esters and other aspects.Related Products of 2567-29-5

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

On March 31, 2020, Rodriguez-Cruz, Mario A.; Hernandez-Ortega, Simon; Valdes, Hugo; Rufino-Felipe, Ernesto; Morales-Morales, David published an article.Category: bromides-buliding-blocks The title of the article was C-S cross-coupling catalyzed by a series of easily accessible, well defined Ni(II) complexes of the type [(NHC)Ni(Cp)(Br)]. And the article contained the following:

The synthesis, characterization and catalytic evaluation of a series of NHC-Ni(II) complexes I [R = Me, n-Bu, Bn] bearing a phthalimide fragment and a cyclopentadienyl (Cp) ligand was reported. The complexes were evaluated in C-S couplings of iodobenzene and a range of thiols to give thioethers R1-S-R2 [R1 = Ph; R2 = t-Bu, 4-FC6H4, 2-naphthyl, etc.]. The reactions were carried out using a catalyst loading of 5 mol % in DMF during 0.5-19 h. Complex I [R = n-Bu] was the one exhibited the best activity for these transformations yielding up to 96% of products in 0.5 h. The experimental process involved the reaction of 2-(2-Bromoethyl)isoindoline-1,3-dione(cas: 574-98-1).Category: bromides-buliding-blocks

The Article related to nhc based nickel complex preparation, thioether preparation, thiol iodobenzene carbon sulfur cross coupling nickel catalyst, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Phenols, Thiophenols, and Derivatives Including Phenol and Thiophenol Ethers and Esters and other aspects.Category: bromides-buliding-blocks

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

On July 31, 2022, Jing, Ke; Wei, Ming-Kai; Yan, Si-Shun; Liao, Li-Li; Niu, Ya-Nan; Luo, Shu-Ping; Yu, Bo; Yu, Da-Gang published an article.Application In Synthesis of 4-(Bromomethyl)-1,1′-biphenyl The title of the article was Visible-light photoredox-catalyzed carboxylation of benzyl halides with CO2: Mild and transition-metal-free. And the article contained the following:

The visible-light photoredox-catalyzed carboxylation of benzyl chlorides and bromides with CO2 has been reported. With inexpensive organic dyes as photocatalysts and amines as electron donors, this carboxylation proceeds well in the absence of sensitive organometallic reagents, transition metal catalysts, or metallic reductants. A wide range of com. available and inexpensive benzyl halides undergo such carboxylation to give valuable aryl acetic acids, including several pharmaceutical mols. and drug precursors, in moderate to high yields. Moreover, this reaction features mild reaction conditions (one atm. pressure of CO2 and room temperature), broad substrate scope, good functional group tolerance, easy scalability, and low catalyst loading, thus providing an efficient approach for the assembly of aryl acetic acids. The experimental process involved the reaction of 4-(Bromomethyl)-1,1′-biphenyl(cas: 2567-29-5).Application In Synthesis of 4-(Bromomethyl)-1,1′-biphenyl

The Article related to aryl acetic acid preparation visible light, benzyl chloride bromide carbon dioxide carboxylation photoredox catalyst, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Carboxylic Acids and Peroxycarboxylic Acids and Their Sulfur-Containing Analogs and Salts and other aspects.Application In Synthesis of 4-(Bromomethyl)-1,1′-biphenyl

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

On November 30, 1989, Porwisiak, Jacek; Dmowski, Wojciech published an article.Related Products of 41819-13-0 The title of the article was An improved synthesis of dihalopyromellitic acids. And the article contained the following:

Durene (I, R = H) is halogenated to give I (R = Cl, Br), followed by oxidation with HNO3 and a catalytic amount of NH4VO3 to obtain a mixture of polycarboxylic acids. Subsequent oxidation with KMnO4 gives the title compounds II (R = Cl, Br) in 50-52% yield. The experimental process involved the reaction of 3,6-Dibromobenzene-1,2,4,5-tetracarboxylic acid(cas: 41819-13-0).Related Products of 41819-13-0

The Article related to chloropyromellitic acid, bromopyromellitic acid, halopyromellitic acid, oxidation halodurene, durene chlorination bromination, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Carboxylic Acids and Peroxycarboxylic Acids and Their Sulfur-Containing Analogs and Salts and other aspects.Related Products of 41819-13-0

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

On September 3, 2020, He, Chen; Han, Wen-Yong; Cui, Bao-Dong; Wan, Nan-Wei; Chen, Yong-Zheng published an article.Reference of 4-(Bromomethyl)-1,1′-biphenyl The title of the article was Efficient Assembly of Molecular Complexity Enabled by Palladium-Catalyzed Heck Coupling/C(sp2)-H Activation/ C(sp3)-H Activation Cascade. And the article contained the following:

A palladium-catalyzed [2+2+1] annulation among 3-iodochromones, benzyl bromides, and norbornene has been developed. This annulation consists of a domino sequence involving Heck coupling/C(sp2)-H activation/C(sp3)-H activation, affording a variety of complex chromone derivatives I (R = H, 6-Me, 7-F, etc.; R1 = C6H5, 3-MeC6H4, 4-FC6H4, etc.) bearing five contiguous tertiary carbon centers in up to 94% yield and 99:1 dr. Interestingly, the diastereoselectivity could be switched by fine-tuning the solvent, in which endo isomer and exo isomer were obtained using mesitylene/CH3CN and mesitylene, resp. The experimental process involved the reaction of 4-(Bromomethyl)-1,1′-biphenyl(cas: 2567-29-5).Reference of 4-(Bromomethyl)-1,1′-biphenyl

The Article related to chromone preparation diastereoselective palladium catalyst, iodochromone benzyl bromide norbornene heck coupling carbon hydrogen activation, Heterocyclic Compounds (One Hetero Atom): Benzopyrans (Including Coumarins, Isocoumarins, Chromones, Benzopyrones, Dibenzopyrans, and Other Arenopyrans) and other aspects.Reference of 4-(Bromomethyl)-1,1′-biphenyl

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

On January 31, 2022, Gao, Yong; Fu, Zhenda; Wu, Di; Yin, Hongquan; Chen, Fu-Xue published an article.Formula: C13H11Br The title of the article was Organocatalyzed Asymmetric Tandem Intramolecular oxa-Michael Addition/Electrophilic Thiocyanation: Synthesis of Chiral α-Thiocyanato Flavanones. And the article contained the following:

An efficient bifunctional cinchona alkaloids-catalyzed asym. tandem intramol. oxa-Michael addition/electrophilic thiocyanation of alkylidene β-ketoesters with N-thiocyanatosuccinimide (NTS) was developed. A series of chiral α-thiocyanato flavanones containing two vicinal stereocenters including an all-carbon quaternary center I [R1 = H, 7-Me, 6-Cl; R2 = Ph, 2-naphthyl, 2-thienyl, etc.; R3 = Me, Et, t-Bu] were prepared in good yields with excellent diastereo- and enantioselectivities (up to 97% ee) under mild conditions, and a successful scale up preparation of our protocol was also demonstrated. The experimental process involved the reaction of 4-(Bromomethyl)-1,1′-biphenyl(cas: 2567-29-5).Formula: C13H11Br

The Article related to chiral thiocyanato flavanone preparation, alkylidene ketoester thiocyanatosuccinimide asym tandem michael addition thiocyanation organocatalyst, Heterocyclic Compounds (One Hetero Atom): Benzopyrans (Including Coumarins, Isocoumarins, Chromones, Benzopyrones, Dibenzopyrans, and Other Arenopyrans) and other aspects.Formula: C13H11Br

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary