Fulopova, Veronika’s team published research in ACS Combinatorial Science in 2012 | CAS: 59290-82-3

3-Nitroisonicotinic acid(cas: 59290-82-3) belongs to pyridine. Pyridine, its benzo and pyridine-based compounds play diverse roles in organic chemistry. As ligands, solvents, and catalysts they facilitate reactions; thus descriptions of these new ligands and their applications abound each year.Application In Synthesis of 3-Nitroisonicotinic acid

Fulopova, Veronika; Gucky, Tomas; Grepl, Martin; Soural, Miroslav published their research in ACS Combinatorial Science on December 10 ,2012. The article was titled 《Solid-Phase Synthesis of Trisubstituted Benzo[1,4]-Diazepin-5-one Derivatives》.Application In Synthesis of 3-Nitroisonicotinic acid The article contains the following contents:

Solid-phase synthesis of 3,4-dihydro-benzo[e][1,4]diazepin-5-ones with three diversity positions is described. Various primary amines were used as the starting material and immobilized on the polystyrene resin equipped with different acid-labile linkers. Polymer-supported amines were converted to α-amino ketones with the use of their sulfonylation with the 4-nitrobenzenesulfonyl chloride (4-Nos-Cl) and subsequent alkylation with α-bromo ketones. After the cleavage of the 4-Nos group, the corresponding α-amino ketones were acylated with various o-nitrobenzoic acids. Reduction of the nitro group followed by spontaneous on-resin ring closure gave the target immobilized benzodiazepines. After acid-mediated cleavage the products were obtained in very good crude purity and satisfactory yields, which makes the developed method applicable for simple library synthesis of the corresponding derivatives in a combinatorial fashion. In the part of experimental materials, we found many familiar compounds, such as 3-Nitroisonicotinic acid(cas: 59290-82-3Application In Synthesis of 3-Nitroisonicotinic acid)

3-Nitroisonicotinic acid(cas: 59290-82-3) belongs to pyridine. Pyridine, its benzo and pyridine-based compounds play diverse roles in organic chemistry. As ligands, solvents, and catalysts they facilitate reactions; thus descriptions of these new ligands and their applications abound each year.Application In Synthesis of 3-Nitroisonicotinic acid

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Deady, L. W.’s team published research in Australian Journal of Chemistry in 1971 | CAS: 29681-39-8

Methyl 5-methoxypicolinate(cas: 29681-39-8) belongs to pyridine. Pyridine, its benzo and pyridine-based compounds play diverse roles in organic chemistry. As ligands, solvents, and catalysts they facilitate reactions; thus descriptions of these new ligands and their applications abound each year.Related Products of 29681-39-8

In 1971,Australian Journal of Chemistry included an article by Deady, L. W.; Shanks, R. A.; Campbell, Arthur Derek; Chooi, S. Y.. Related Products of 29681-39-8. The article was titled 《Synthesis of some substituted methyl pyridinecarboxylates. II. Methyl 4-substituted picolinates, methyl 5-substituted picolinates, and methyl 5-substituted nicotinates》. The information in the text is summarized as follows:

The preparation of substituted Me pyridinecarboxylates is described. Me 4-X-substituted picolinates and methyl 5-X-substituted picolinates (X = NO2, Br, MeO, Me2N) are prepared from 2-picoline via 4-nitro-2-picoline N-oxide and 2-amino-5-nitropyridine, resp. Me 5-X-substituted nicotinates (X = Br, MeO, Me2N) are prepared from 5-bromonicotinic acid. Preparations of Me 4-methylpicolinate and Me 5-methylnicotinate from the corresponding lutidines and Me 5-methylpicolinate from 2-amino-5-methylpyridine are described. In the experiment, the researchers used many compounds, for example, Methyl 5-methoxypicolinate(cas: 29681-39-8Related Products of 29681-39-8)

Methyl 5-methoxypicolinate(cas: 29681-39-8) belongs to pyridine. Pyridine, its benzo and pyridine-based compounds play diverse roles in organic chemistry. As ligands, solvents, and catalysts they facilitate reactions; thus descriptions of these new ligands and their applications abound each year.Related Products of 29681-39-8

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Kader, Thomas’s team published research in Chemistry – A European Journal in 2019 | CAS: 39856-58-1

2-Bromopyridin-3-amine(cas: 39856-58-1) belongs to anime. Hydrogen peroxide (H2O2) and peroxy acids generally add an oxygen atom to the nitrogen of amines. With primary amines, this step is normally followed by further oxidation, leading to nitroso compounds, RNO, or nitro compounds, RNO2. Secondary amines are converted to hydroxylamines, R2NOH, and tertiary amines to amine oxides, R3NO.Related Products of 39856-58-1

In 2019,Chemistry – A European Journal included an article by Kader, Thomas; Stoeger, Berthold; Froehlich, Johannes; Kautny, Paul. Related Products of 39856-58-1. The article was titled 《Azaindolo[3,2,1-jk]carbazoles: New Building Blocks for Functional Organic Materials》. The information in the text is summarized as follows:

The preparation and characterization of 12 azaindolo[3,2,1-jk]carbazoles, e.g., I was presented. Ring-closing C-H activation allowed for the convenient preparation of six singly and six doubly nitrogen-substituted indolo[3,2,1-jk]carbazole derivatives in which ten of the materials had not been described in the literature before. The detailed photophys. and electrochem. characterization of the developed materials revealed a significant impact of the incorporation of pyridine-like nitrogen into the fully planar indolo[3,2,1-jk]carbazole backbone. Furthermore, the nitrogen position decisively impacted intermol. hydrogen bonding and thus the solid-state alignment. Ultimately, the versatility of the azaindolo[3,2,1-jk]carbazoles scaffold makes this class of materials an attractive new building block for the design of functional organic materials. In the part of experimental materials, we found many familiar compounds, such as 2-Bromopyridin-3-amine(cas: 39856-58-1Related Products of 39856-58-1)

2-Bromopyridin-3-amine(cas: 39856-58-1) belongs to anime. Hydrogen peroxide (H2O2) and peroxy acids generally add an oxygen atom to the nitrogen of amines. With primary amines, this step is normally followed by further oxidation, leading to nitroso compounds, RNO, or nitro compounds, RNO2. Secondary amines are converted to hydroxylamines, R2NOH, and tertiary amines to amine oxides, R3NO.Related Products of 39856-58-1

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Khavasi, Hamid Reza’s team published research in Crystal Growth & Design in 2019 | CAS: 112881-51-3

4′-(4-Pyridyl)-2,2′:6′,2”-terpyridine(cas: 112881-51-3) belongs to pyridine derivatives. Several pyridine derivatives play important roles in biological systems. While its biosynthesis is not fully understood, nicotinic acid (vitamin B3) occurs in some bacteria, fungi, and mammals. HPLC of Formula: 112881-51-3

Khavasi, Hamid Reza; Esmaeili, Maryam published their research in Crystal Growth & Design on August 7 ,2019. The article was titled 《Case Study of the Correlation between Metallogelation Ability and Crystal Packing》.HPLC of Formula: 112881-51-3 The article contains the following contents:

In the present paper, in order to find the correlation between the mol. structure and the intermol. interaction patterns in the crystalline state and the corresponding gelating or nongelating behavior, two structurally related sets of copper complexes, including (CuCl2[L2pyTerpy]), 1, (CuCl2[L3pyTerpy]), 2, and (CuCl2[L4pyTerpy]), 3, (where LnpyTerpy is 4′-(n-pyridyl)-2,2′,6′,2”-terpyridine) as the first set and (CuCl2[L2pydipyz-py]), 4, (CuCl2[L3pydipyz-py]), 5, and (CuCl2[L4pydipyz-py]), 6, (where Lnpydipyz-py is 4-(n-pyridyl)-2,6-dipyrazin-2-yl-pyridine) as the second one, have been synthesized, and their crystal packing as well as gelating properties have been investigated. Results show that although these two sets are structurally similar the first set forms a metastable hydrogel, while the second one is unable to form a gel. To investigate the reasons, we employed Hirshfeld surface anal. and examined the differences in their packing arrangements, which suggest hydrogen bonding arranged into the three-dimensional network is a preferred mode of packing for the crystalline solid but is unfavorable for gel formation. In the part of experimental materials, we found many familiar compounds, such as 4′-(4-Pyridyl)-2,2′:6′,2”-terpyridine(cas: 112881-51-3HPLC of Formula: 112881-51-3)

4′-(4-Pyridyl)-2,2′:6′,2”-terpyridine(cas: 112881-51-3) belongs to pyridine derivatives. Several pyridine derivatives play important roles in biological systems. While its biosynthesis is not fully understood, nicotinic acid (vitamin B3) occurs in some bacteria, fungi, and mammals. HPLC of Formula: 112881-51-3

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Suga, Hiroyuki’s team published research in Journal of Organic Chemistry in 2015 | CAS: 410092-98-7

2,6-Bis((4S,5S)-4,5-diphenyl-4,5-dihydrooxazol-2-yl)pyridine(cas: 410092-98-7) belongs to pyridine derivatives. Several pyridine derivatives play important roles in biological systems. While its biosynthesis is not fully understood, nicotinic acid (vitamin B3) occurs in some bacteria, fungi, and mammals. Safety of 2,6-Bis((4S,5S)-4,5-diphenyl-4,5-dihydrooxazol-2-yl)pyridine

Suga, Hiroyuki; Sekikawa, Yurie; Misawa, Shunta; Kinugawa, Daito; Oda, Rinnosuke; Itoh, Kennosuke; Toda, Yasunori; Kiyono, Ryotaro published an article in Journal of Organic Chemistry. The title of the article was 《Chiral Lewis Acid-Catalyzed Enantioselective Cycloadditions between Indoles and Cyclic Carbonyl Ylides Derived from Diazodiketone or Diazoketoester Derivatives》.Safety of 2,6-Bis((4S,5S)-4,5-diphenyl-4,5-dihydrooxazol-2-yl)pyridine The author mentioned the following in the article:

Asym. 1,3-dipolar cycloaddition reactions between N-methylindoles and several cyclic carbonyl ylides that were derived from diazodiketone or diazoketoester precursors in the presence of both achiral Rh and chiral lanthanoid metal catalysts are described. For the six-membered cyclic carbonyl ylides derived from 1-diazo-5-aryl-2,5-pentanedione precursors, the cycloaddition reactions were carried out using Rh2(OAc)4 (2 mol %) and the chiral Pybox-Ph2-Lu(OTf)3 complex (10 mol %) as catalysts, resulting in high enantioselectivities (83% to >98% ee (exo)) along with relatively good exo-selectivities (exo:endo = 65:35 to 94:6) and yields (63-85%). For the five-membered cyclic carbonyl ylide derived from 1-diazo-2,4-pentanedione precursor, the cycloaddition reaction with 5-bromo-1-methylindole was carried out in the presence of Rh2(OAc)4 (2 mol %) and the chiral Pybox-Ph2-Er(OTf)3 complex (30 mol %) as catalysts, resulting in relatively good enantioselectivity (78% ee) and endo-selectivity (endo:exo = 81:19). The experimental process involved the reaction of 2,6-Bis((4S,5S)-4,5-diphenyl-4,5-dihydrooxazol-2-yl)pyridine(cas: 410092-98-7Safety of 2,6-Bis((4S,5S)-4,5-diphenyl-4,5-dihydrooxazol-2-yl)pyridine)

2,6-Bis((4S,5S)-4,5-diphenyl-4,5-dihydrooxazol-2-yl)pyridine(cas: 410092-98-7) belongs to pyridine derivatives. Several pyridine derivatives play important roles in biological systems. While its biosynthesis is not fully understood, nicotinic acid (vitamin B3) occurs in some bacteria, fungi, and mammals. Safety of 2,6-Bis((4S,5S)-4,5-diphenyl-4,5-dihydrooxazol-2-yl)pyridine

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Tsubogo, Tetsu’s team published research in Chemistry – An Asian Journal in 2013 | CAS: 410092-98-7

2,6-Bis((4S,5S)-4,5-diphenyl-4,5-dihydrooxazol-2-yl)pyridine(cas: 410092-98-7) belongs to pyridine derivatives. The ring atoms in the pyridine molecule are sp2-hybridized. The nitrogen is involved in the π-bonding aromatic system using its unhybridized p orbital. Synthetic Route of C35H27N3O2 Pyridine has a conjugated system of six π electrons that are delocalized over the ring.

The author of 《Chiral Calcium Iodide for Asymmetric Mannich-type Reactions of Malonates with Imines Providing β-Aminocarbonyl Compounds》 were Tsubogo, Tetsu; Shimizu, Shota; Kobayashi, Shu. And the article was published in Chemistry – An Asian Journal in 2013. Synthetic Route of C35H27N3O2 The author mentioned the following in the article:

We have developed a novel chiral calcium iodide catalyst prepared from CaI2 and pybox [2,6-bis(2-oxazolinyl)pyridine] that is stable under moisture and oxygen. This catalyst was applied to catalytic asym. Mannich-type reactions of malonates with both N-Boc-protected aromatic and aliphatic imines, and gave moderate to high yields of β-aminocarbonyl compounds with high enantioselectivities. The Mannich adduct was also successfully converted into an α-hydroxy β-amino acid derivative In the experiment, the researchers used 2,6-Bis((4S,5S)-4,5-diphenyl-4,5-dihydrooxazol-2-yl)pyridine(cas: 410092-98-7Synthetic Route of C35H27N3O2)

2,6-Bis((4S,5S)-4,5-diphenyl-4,5-dihydrooxazol-2-yl)pyridine(cas: 410092-98-7) belongs to pyridine derivatives. The ring atoms in the pyridine molecule are sp2-hybridized. The nitrogen is involved in the π-bonding aromatic system using its unhybridized p orbital. Synthetic Route of C35H27N3O2 Pyridine has a conjugated system of six π electrons that are delocalized over the ring.

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Wu, Chunjiang’s team published research in Medicinal Chemistry Research in 2018 | CAS: 1158763-55-3

5-(3-Fluorophenyl)picolinic acid(cas: 1158763-55-3) belongs to pyridine derivatives. The ring atoms in the pyridine molecule are sp2-hybridized. The nitrogen is involved in the π-bonding aromatic system using its unhybridized p orbital. HPLC of Formula: 1158763-55-3The lone pair is in an sp2 orbital, projecting outward from the ring in the same plane as the σ bonds.

Wu, Chunjiang; Xu, Shan; Guo, Yuping; Wu, Jielian; Luo, Rong; Wang, Wenhui; Tu, Yuanbiao; Le Chen; Zhu, Wufu; Zheng, Pengwu published an article on February 28 ,2018. The article was titled 《Design, synthesis and biological evaluation of phenylpicolinamide sorafenib derivatives as antitumor agents》, and you may find the article in Medicinal Chemistry Research.HPLC of Formula: 1158763-55-3 The information in the text is summarized as follows:

Two series of phenylpicolinamide sorafenib derivatives (14a-k, 15a-k) were designed and synthesized. They were evaluated for IC50 values against three cancer cell lines (A549, Hela, and MCF-7) and VEGFR2/KDR, BRAF, and CRAF kinases. Fourteen target compounds showed moderate to excellent cytotoxicity activity against the different cancer cells with potency from the single-digit μM to nanomole range. What’s more, six of them were equal to more potent than sorafenib against one or more cell lines. Most of the compounds showed bad activity against VEGFR2/KDR, BRAF, or CRAF kinases. The most promising compound 15f showed strong antitumor activities against A549 and MCF-7 cell lines with IC50 values of 5.43 ± 0.74 and 0.62 ± 0.21 μM, which were 1.29-6.79-fold more active than sorafenib (6.53 ± 0.82, 4.21 ± 0.62 μM), resp. and it exhibited moderate IC50 (7.1 μM) than 14f (IC50 = 3.1 μM). Structure-activity relationships (SARs) and docking studies indicated that replacement of diarylurea of sorafenib with phenylpicolinamide moiety benefits to the activity. The position of aryl group and the substitutions of aryl group have a great influence on antitumor activity and selectivity. Small volume groups of aryl group such as (substituted) alkyl groups (-CH3, -CF3), halogen atoms (-F) were favorable to the cytotoxicity. Exact action mechanism of target compounds is not quite clear and further study will be carried out to identify the target in near future. After reading the article, we found that the author used 5-(3-Fluorophenyl)picolinic acid(cas: 1158763-55-3HPLC of Formula: 1158763-55-3)

5-(3-Fluorophenyl)picolinic acid(cas: 1158763-55-3) belongs to pyridine derivatives. The ring atoms in the pyridine molecule are sp2-hybridized. The nitrogen is involved in the π-bonding aromatic system using its unhybridized p orbital. HPLC of Formula: 1158763-55-3The lone pair is in an sp2 orbital, projecting outward from the ring in the same plane as the σ bonds.

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Gao, Zhaobing’s team published research in Journal of Biological Chemistry in 2010 | CAS: 13534-97-9

6-Bromopyridin-3-amine(cas: 13534-97-9) belongs to anime. Reduction of nitro compounds, RNO2, by hydrogen or other reducing agents produces primary amines cleanly (i.e., without a mixture of products), but the method is mostly used for aromatic amines because of the limited availability of aliphatic nitro compounds. Reduction of nitriles and oximes (R2C=NOH) also yields primary amines.Product Details of 13534-97-9

In 2010,Gao, Zhaobing; Zhang, Tangzhi; Wu, Meng; Xiong, Qiaojie; Sun, Haiyan; Zhang, Yinan; Zu, Liansuo; Wang, Wei; Li, Min published 《Isoform-specific Prolongation of Kv7 (KCNQ) Potassium Channel Opening Mediated by New Molecular Determinants for Drug-Channel Interactions》.Journal of Biological Chemistry published the findings.Product Details of 13534-97-9 The information in the text is summarized as follows:

Kv7 channels, especially Kv7.2 (KCNQ2) and Kv7.3 (KCNQ3), are key determinants for membrane excitability in the brain. Some chem. modulators of KCNQ channels are in development for use as anti-epileptic drugs, such as retigabine (D-23129, N-(2-amino-4-(4-fluorobenzylamino)-phenyl)), which was recently approved for clin. use. In addition, several other compounds were also reported to potentiate activity of the Kv7 channels. It is therefore of interest to investigate compound-channel interactions, so that more insights may be gained to aid future development of therapeutics. We have conducted a screen of 20,000 compounds for KCNQ2 potentiators using rubidium flux combined with at. absorption spectrometry. Here, we report the characterization of a series of new structures that display isoform specificity and induce a marked reduction of deactivation distinct from that of retigabine. Furthermore, KCNQ2(W236L), a previously reported mutation that abolishes sensitivity to retigabine, remains fully sensitive to these compounds This result, together with mutagenesis and other studies, suggests that the reported compounds confer a unique mode of action and involve new mol. determinants on the channel protein, consistent with the idea of recognizing a new site on channel protein. The results came from multiple reactions, including the reaction of 6-Bromopyridin-3-amine(cas: 13534-97-9Product Details of 13534-97-9)

6-Bromopyridin-3-amine(cas: 13534-97-9) belongs to anime. Reduction of nitro compounds, RNO2, by hydrogen or other reducing agents produces primary amines cleanly (i.e., without a mixture of products), but the method is mostly used for aromatic amines because of the limited availability of aliphatic nitro compounds. Reduction of nitriles and oximes (R2C=NOH) also yields primary amines.Product Details of 13534-97-9

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Ghiron, Chiara’s team published research in Journal of Medicinal Chemistry in 2010 | CAS: 13534-97-9

6-Bromopyridin-3-amine(cas: 13534-97-9) belongs to anime. Many important products require amines as part of their syntheses. Methylamine is utilized in the production of the analgesic meperidine (trade name Demerol) and the photographic developer Metol (trademark), and dimethylamine is used in the synthesis of the antihistamine diphenhydramine (trade name Benadryl), the solvent dimethylformamide (DMF), and the rocket propellant 1,1-dimethylhydrazine. The synthesis of the insect repellent N,N-diethyl-m-toluamide (DEET) incorporates diethylamine while that of the synthetic fibre Kevlar requires aromatic amines.Application In Synthesis of 6-Bromopyridin-3-amine

In 2010,Ghiron, Chiara; Haydar, Simon N.; Aschmies, Suzan; Bothmann, Hendrick; Castaldo, Cristiana; Cocconcelli, Giuseppe; Comery, Thomas A.; Di, Li; Dunlop, John; Lock, Tim; Kramer, Angela; Kowal, Dianne; Jow, Flora; Grauer, Steve; Harrison, Boyd; La Rosa, Salvatore; Maccari, Laura; Marquis, Karen L.; Micco, Iolanda; Nencini, Arianna; Quinn, Joanna; Robichaud, Albert J.; Roncarati, Renza; Scali, Carla; Terstappen, Georg C.; Turlizzi, Elisa; Valacchi, Michela; Varrone, Maurizio; Zanaletti, Riccardo; Zanelli, Ugo published 《Novel Alpha-7 Nicotinic Acetylcholine Receptor Agonists Containing a Urea Moiety: Identification and Characterization of the Potent, Selective, and Orally Efficacious Agonist 1-[6-(4-Fluorophenyl)pyridin-3-yl]-3-(4-piperidin-1-ylbutyl) Urea (SEN34625/WYE-103914)》.Journal of Medicinal Chemistry published the findings.Application In Synthesis of 6-Bromopyridin-3-amine The information in the text is summarized as follows:

Alpha-7 nicotinic acetylcholine receptor (α7 nAChR) agonists are promising therapeutic candidates for the treatment of cognitive impairment. We report a series of novel, potent small mol. agonists (4-18) of the α7 nAChR deriving from our continuing efforts in the areas of Alzheimer’s disease and schizophrenia. One of the compounds of the series containing a urea moiety (16)(I) was further shown to be a selective agonist of the α7 nAChR with excellent in vitro and in vivo profiles, brain penetration, and oral bioavailability and demonstrated in vivo efficacy in multiple behavioral cognition models. Structural modifications leading to the improved selectivity profile and the biol. evaluation of this series of compounds are discussed. In addition to this study using 6-Bromopyridin-3-amine, there are many other studies that have used 6-Bromopyridin-3-amine(cas: 13534-97-9Application In Synthesis of 6-Bromopyridin-3-amine) was used in this study.

6-Bromopyridin-3-amine(cas: 13534-97-9) belongs to anime. Many important products require amines as part of their syntheses. Methylamine is utilized in the production of the analgesic meperidine (trade name Demerol) and the photographic developer Metol (trademark), and dimethylamine is used in the synthesis of the antihistamine diphenhydramine (trade name Benadryl), the solvent dimethylformamide (DMF), and the rocket propellant 1,1-dimethylhydrazine. The synthesis of the insect repellent N,N-diethyl-m-toluamide (DEET) incorporates diethylamine while that of the synthetic fibre Kevlar requires aromatic amines.Application In Synthesis of 6-Bromopyridin-3-amine

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Younis, Yassir’s team published research in Journal of Medicinal Chemistry in 2013 | CAS: 13534-97-9

6-Bromopyridin-3-amine(cas: 13534-97-9) belongs to anime. Acylation is one of the most important reactions of primary and secondary amines; a hydrogen atom is replaced by an acyl group (a group derived from an acid, such as RCOOH or RSO3H, by removal of ―OH, such as RC(=O)―, RS(O)2―, and so on). Reagents may be acid chlorides (RCOC1, RSO2C1), anhydrides ((RCO)2O), or even esters (RCOOR′); the products are amides of the corresponding acids.HPLC of Formula: 13534-97-9

In 2013,Younis, Yassir; Douelle, Frederic; Gonzalez Cabrera, Diego; Le Manach, Claire; Nchinda, Aloysius T.; Paquet, Tanya; Street, Leslie J.; White, Karen L.; Zabiulla, K. Mohammed; Joseph, Jayan T.; Bashyam, Sridevi; Waterson, David; Witty, Michael J.; Wittlin, Sergio; Charman, Susan A.; Chibale, Kelly published 《Structure-Activity-Relationship Studies around the 2 Amino Group and Pyridine Core of Antimalarial 3,5-Diarylaminopyridines Lead to a Novel Series of Pyrazine Analogues with Oral in Vivo Activity》.Journal of Medicinal Chemistry published the findings.HPLC of Formula: 13534-97-9 The information in the text is summarized as follows:

Replacement of the pyridine core of antimalarial 3,5-diaryl-2-aminopyridines led to the identification of a novel series of pyrazine analogs with potent oral antimalarial activity. However, other changes to the pyridine core and replacement or substitution of the 2-amino group led to loss of antimalarial activity. The 3,5-diaryl-2-aminopyrazine series showed impressive in vitro antiplasmodial activity against the K1 (multidrug resistant) and NF54 (sensitive) strains of Plasmodium falciparum in the nanomolar IC50 range of 6-94 nM while also demonstrating good in vitro metabolic stability in human liver microsomes. In the Plasmodium berghei mouse model, this series generally exhibited good efficacy at low oral doses. One of the frontrunner compounds, (I), displayed potent in vitro antiplasmodial activity with IC50 values of 8.4 and 10 nM against the K1 and NF54 strains, resp. When evaluated in P. berghei-infected mice, compound I was completely curative at an oral dose of 4×10 mg/kg. In the experimental materials used by the author, we found 6-Bromopyridin-3-amine(cas: 13534-97-9HPLC of Formula: 13534-97-9)

6-Bromopyridin-3-amine(cas: 13534-97-9) belongs to anime. Acylation is one of the most important reactions of primary and secondary amines; a hydrogen atom is replaced by an acyl group (a group derived from an acid, such as RCOOH or RSO3H, by removal of ―OH, such as RC(=O)―, RS(O)2―, and so on). Reagents may be acid chlorides (RCOC1, RSO2C1), anhydrides ((RCO)2O), or even esters (RCOOR′); the products are amides of the corresponding acids.HPLC of Formula: 13534-97-9

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem