pyrazoles-derivatives

Inhibitory effects of pyrazoles on soil nitrification: effects of chemical structure was written by Shi, Yunfeng;Zhang, Lili;Wu, Zhijie. And the article was included in Fresenius Environmental Bulletin in 2012.COA of Formula: C5H7ClN2 This article mentions the following:

Pyrazoles are nitrification inhibitors with good inhibitory effects. In this study, chem. structure of pyrazoles and its relationship with nitrification inhibitory effects were studied through aerobic incubation, and the optimal concentrations of three nitrification inhibitors with better nitrification inhibitory effects were explored, including 3,4-dimethylpyrazole phosphate (DMPP), 1-carboxamide-3-methylpyrazole (CMP), and 4-chloro-3-methylpyrazole (ClMP). The results showed that all the pyrazoles could effectively inhibit NH₄⁺ oxidation in soils. Specifically, inhibitory effects of 3-methylpyrazole, 3,4-dimethylpyrazole, 4-chloro-3-methylpyrazole and their derivatives were the best. When the 4-position was substituted by chlorine atoms, nitrification inhibitory effects of pyrazoles could be significantly improved, which were not affected by the substitution at 1-position (hydroxymethylation and amidation) and neutralization. Nitrification inhibitory rate and inhibitory duration were increased with increasing consumptions of nitrification inhibitor pyrazoles. The optimal concentrations of three nitrification inhibitors with better nitrification inhibitory effects, including DMPP, CMP and ClMP, should be controlled in the range of 0.25-1.0% of N application, and the nitrification duration was about 56 days. In the experiment, the researchers used many compounds, for example, 4-Chloro-3,5-dimethyl-1H-pyrazole (cas: 15953-73-8COA of Formula: C5H7ClN2).

4-Chloro-3,5-dimethyl-1H-pyrazole (cas: 15953-73-8) belongs to pyrazole derivatives. An alternative way to synthesize multisubstituted pyrazoles is the Csingle bondH arylation of simple pyrazoles. Pyrazole rings have been used as core components of several leading non-steroidal anti-inflammatory drugs (NSAIDs) and antihypertensive drugs. It has also been found to be useful as a bifunctional ligand for metal catalysis.COA of Formula: C5H7ClN2

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Development of a new cascade reaction for convergent synthesis of pyrazolo[1,5-a]quinoline derivatives under transition-metal-free conditions was written by Kato, Jun-ya;Aoyama, Hiroshi;Yokomatsu, Tsutomu. And the article was included in Organic & Biomolecular Chemistry in 2013.Product Details of 15953-73-8 This article mentions the following:

A method for the synthesis of pyrazolo[1,5-a]quinolines under the transition-metal-free conditions has been developed. This method involves a novel combination of aromatic nucleophilic substitution and Knoevenagel condensation reactions to give pyrazolo[1,5-a]quinolines. In the experiment, the researchers used many compounds, for example, 4-Chloro-3,5-dimethyl-1H-pyrazole (cas: 15953-73-8Product Details of 15953-73-8).

4-Chloro-3,5-dimethyl-1H-pyrazole (cas: 15953-73-8) belongs to pyrazole derivatives. Pyrazoles, a five-membered heterocycle containing two adjacent nitrogen atoms, are the core structures found in a number of molecules that possess a wide range of pharmaceutical and agricultural activities. Protonation of pyrazole in strong acid leads to pyrazolium cations, which undergo electrophilic substitution preferentially at C3 rather than C4. The pyrazole anion is not reactive toward nucleophiles but is mostly reactive to electrophiles.Product Details of 15953-73-8

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Dinitration of 1-methylpyrazole: 1-methyl-3,4-dinitropyrazole was written by Grimmett, M. Ross;Lim, K. H. Richard. And the article was included in Australian Journal of Chemistry in 1978.Quality Control of 1-Methyl-3-nitro-1H-pyrazole This article mentions the following:

Nitration in 80% H₂SO₄ of 1-methylpyrazole gives 1-methyl-4-nitropyrazole and 1-methyl-3,4-dinitropyrazole in a 4:1 ratio. The dinitro compound is also formed by nitration of 1-methyl-3-nitropyrazole. In the experiment, the researchers used many compounds, for example, 1-Methyl-3-nitro-1H-pyrazole (cas: 54210-32-1Quality Control of 1-Methyl-3-nitro-1H-pyrazole).

1-Methyl-3-nitro-1H-pyrazole (cas: 54210-32-1) belongs to pyrazole derivatives. As is the case with imidazoles, the pyrazole ring offers many opportunities to create new multiring systems that incorporate this heterocycle. Protonation of pyrazole in strong acid leads to pyrazolium cations, which undergo electrophilic substitution preferentially at C3 rather than C4. The pyrazole anion is not reactive toward nucleophiles but is mostly reactive to electrophiles.Quality Control of 1-Methyl-3-nitro-1H-pyrazole

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Synthesis of 1H-pyrazolo[3,4-b]pyridine 5-ketones was written by Denzel, Theodor;Hoehn, Hans. And the article was included in Archiv der Pharmazie (Weinheim, Germany) in 1976.Recommanded Product: 3528-58-3 This article mentions the following:

Pyrazolopyridine ketones I [R1 = Me, R5C6H4 (R5 = H, 3-, 4-Cl, 4-Me, 4-MeO), R2 = H, Me, R3 = Et, furfuryl, Me2CH, CH2Ph, H, R4 = H; R1 = Ph, R2 = H, R3 = furfuryl, R4 = Me] were prepared and converted to analogs. EtO2CCH2COR1 reacted with R2C(OEt)3 to give 45-73% β-oxo esters EtO2CC(COR1):CR2OEt which condensed with 5-aminopyrazoles in a modified Gould-Jacobs reaction to give 55-95% enamines II. These cyclized at 250-300° to give 45-79% I. I were alkylated to give III (R6 = Et, CH2CH2CHMe2) or chlorinated to the 4-Cl analogs, which reacted with amines to give IV (R7 = CHMeEt, 2-pyrimidinyl, Bu, H, Ph). Since the preparation of necessary EtO2CCH2COR1 was sometimes difficult, III (R1 = Et, Bu, decyl, R2 = R4 = H, R3 = R6 = Et) were prepared from the corresponding III (R1 = Cl) and R1MgX-CdCl2. In the experiment, the researchers used many compounds, for example, 1-Ethyl-1H-pyrazol-5-amine (cas: 3528-58-3Recommanded Product: 3528-58-3).

1-Ethyl-1H-pyrazol-5-amine (cas: 3528-58-3) belongs to pyrazole derivatives. The strategies for the synthesis of pyrazoles generally can be applied for the construction of indazoles. Pyrazole rings have been used as core components of several leading non-steroidal anti-inflammatory drugs (NSAIDs) and antihypertensive drugs. It has also been found to be useful as a bifunctional ligand for metal catalysis.Recommanded Product: 3528-58-3

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Design and Synthesis of Highly Potent and Isoform Selective JNK3 Inhibitors: SAR Studies on Aminopyrazole Derivatives was written by Zheng, Ke;Iqbal, Sarah;Hernandez, Pamela;Park, HaJeung;LoGrasso, Philip V.;Feng, Yangbo. And the article was included in Journal of Medicinal Chemistry in 2014.COA of Formula: C4H5N3O2 This article mentions the following:

The c-jun N-terminal kinase 3 (JNK3) is expressed primarily in the brain. Numerous reports have shown that inhibition of JNK3 is a promising strategy for treatment of neurodegeneration. The optimization of aminopyrazole-based JNK3 inhibitors with improved potency, isoform selectivity, and pharmacol. properties by structure-activity relationship (SAR) studies utilizing biochem. and cell-based assays, and structure-based drug design is reported. These inhibitors had high selectivity over JNK1 and p38α, minimal cytotoxicity, potent inhibition of 6-OHDA-induced mitochondrial membrane potential dissipation and ROS generation, and good drug metabolism and pharmacokinetic (DMPK) properties for iv dosing. 26n was profiled against 464 kinases and was found to be highly selective hitting only seven kinases with >80% inhibition at 10 μM. Moreover, 26n showed good solubility, good brain penetration, and good DMPK properties. Finally, the crystal structure of 26k in complex with JNK3 was solved at 1.8 Å to explore the binding mode of aminopyrazole based JNK3 inhibitors. In the experiment, the researchers used many compounds, for example, 3-Methyl-4-nitro-1H-pyrazole (cas: 5334-39-4COA of Formula: C4H5N3O2).

3-Methyl-4-nitro-1H-pyrazole (cas: 5334-39-4) belongs to pyrazole derivatives. The strategies for the synthesis of pyrazoles generally can be applied for the construction of indazoles. The presence of both electronegative nitrogen atoms in the pyrazole ring reduces the electron density of the C3- and C5-positions leaving electron density of C4-position unaltered. Thus the C4-position is vulnerable to electrophilic attack. The C3 electrophilic-position may undergo deprotonation in the presence of a strong base leading to ring opening.COA of Formula: C4H5N3O2

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Carbon-13 NMR chemical shifts of N-unsubstituted and N-methylpyrazole derivatives was written by Cabildo, Pilar;Claramunt, Rosa Maria. And the article was included in Organic Magnetic Resonance in 1984.Safety of 3-Methyl-4-nitro-1H-pyrazole This article mentions the following:

¹³C shielding data for 100 derivatives of pyrazole are reported. These include Me, Et, Pr, tert-Bu, Ph, hydroxymethyl, carboxyl, ethoxycarbonyl, cyano, amino, hydrazino, nitro, azido, chloro, bromo and iodo groups as substituents on the ring carbon atoms. In the experiment, the researchers used many compounds, for example, 3-Methyl-4-nitro-1H-pyrazole (cas: 5334-39-4Safety of 3-Methyl-4-nitro-1H-pyrazole).

3-Methyl-4-nitro-1H-pyrazole (cas: 5334-39-4) belongs to pyrazole derivatives. As is the case with imidazoles, the pyrazole ring offers many opportunities to create new multiring systems that incorporate this heterocycle. Pyrazole the presence of this nucleus in pharmacological agents of diverse therapeutic categories such as celecoxib, a potent anti-inflammatory, the antidepressant agent fezolamide have proved the pharmacological potential of the pyrazole moiety. Safety of 3-Methyl-4-nitro-1H-pyrazole

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Inhibitors of HIV-1 attachment. Part 7: Indole-7-carboxamides as potent and orally bioavailable antiviral agents was written by Yeung, Kap-Sun;Qiu, Zhilei;Xue, Quifen;Fang, Haiquan;Yang, Zheng;Zadjura, Lisa;D’Arienzo, Celia J.;Eggers, Betsy J.;Riccardi, Keith;Shi, Pei-Yong;Gong, Yi-Fei;Browning, Marc R.;Gao, Qi;Hansel, Steven;Santone, Kenneth;Lin, Ping-Fang;Meanwell, Nicholas A.;Kadow, John F.. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2013.Name: 1-Ethyl-1H-pyrazol-5-amine This article mentions the following:

A series of substituted carboxamides at the indole C7 position of the previously described 4-fluoro-substituted indole HIV-1 attachment inhibitor I was synthesized and the SAR delineated. Heteroaryl carboxamide inhibitors that exhibited pM potency in the primary cell-based assay against a pseudotype virus expressing a JRFL envelope were identified. The simple Me amide analog II displayed a promising in vitro profile, with its favorable HLM stability and membrane permeability translating into favorable pharmacokinetic properties in preclin. species. In the experiment, the researchers used many compounds, for example, 1-Ethyl-1H-pyrazol-5-amine (cas: 3528-58-3Name: 1-Ethyl-1H-pyrazol-5-amine).

1-Ethyl-1H-pyrazol-5-amine (cas: 3528-58-3) belongs to pyrazole derivatives. Pyrazole and its derivatives are considered a pharmacologically important active scaffold that possesses almost all types of pharmacological activities. Pyrazoles are commonly used scaffold molecules in drug discovery projects. The use of pyrazole derivatives is based on their analgesic, anti-inflammatory, antipyretic, antiarrhythmic, sedative, muscle relaxant, neuroleptic, anticonvulsant, monoamine oxidase inhibitory, antidiabetic and antibacterial activities.Name: 1-Ethyl-1H-pyrazol-5-amine

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Biaryl substituted hydantoin compounds as TACE inhibitors was written by Yu, Wensheng;Tong, Ling;Kim, Seong Heon;Wong, Michael K. C.;Chen, Lei;Yang, De-Yi;Shankar, Bandarpalle B.;Lavey, Brian J.;Zhou, Guowei;Kosinski, Aneta;Rizvi, Razia;Li, Dansu;Feltz, Robert J.;Piwinski, John J.;Rosner, Kristin E.;Shih, Neng-Yang;Siddiqui, M. Arshad;Guo, Zhuyan;Orth, Peter;Shah, Himanshu;Sun, Jing;Umland, Shelby;Lundell, Daniel J.;Niu, Xiaoda;Kozlowski, Joseph A.. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2010.Related Products of 73387-46-9 This article mentions the following:

We disclose further optimization of hydantoin TNF-α convertase enzyme (TACE) inhibitors. SAR with respect to the non-prime region of TACE active site was explored. A series of biaryl substituted hydantoin compounds was shown to have sub-nanomolar K _i, good rat PK, and good selectivity vs. MMP-1, -2, -3, -7, -9, and -13. In the experiment, the researchers used many compounds, for example, 3-(4-Bromophenyl)-1H-pyrazole (cas: 73387-46-9Related Products of 73387-46-9).

3-(4-Bromophenyl)-1H-pyrazole (cas: 73387-46-9) belongs to pyrazole derivatives. As is the case with imidazoles, the pyrazole ring offers many opportunities to create new multiring systems that incorporate this heterocycle. Pyrazoles and pyrimidines have diverse biological and pharmacological activities. There are a number of antimicrobial compounds containing pyrazole moiety as the core unit. Pyrazofurin is important antimicrobial drug and 2-methylpyrimidine-4-ylamine derivatives I and II were found to be effective inhibitors of Escherichia coli PDHc-E1 with antibacterial and antifungal activity.Related Products of 73387-46-9

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Discovery of a Teraryl Oxazolidinone Compound (S)-N-((3-(3-Fluoro-4-(4-(pyridin-2-yl)-1H-pyrazol-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide Phosphate as a Novel Antimicrobial Agent with Enhanced Safety Profile and Efficacies was written by Yang, Tao;Chen, Gong;Sang, Zitai;Liu, Yuanyuan;Yang, Xiaoyan;Chang, Ying;Long, Haiyue;Wei, Ang;Tang, Jianying;Wang, Zhenling;Li, Guobo;Yang, Shengyong;Zhang, Jingren;Wei, Yuquan;Luo, Youfu. And the article was included in Journal of Medicinal Chemistry in 2015.Synthetic Route of C8H7N3 This article mentions the following:

A series of novel teraryl oxazolidinone compounds was designed, synthesized, and evaluated for their antimicrobial activity and toxicities. The compounds with aromatic N-heterocyclic substituents at the 4-position of pyrazolyl ring showed better antibacterial activity against the tested bacteria than other compounds with different patterns of substitution. Among all potent compounds, I exhibited promising safety profile in MTT assays and in hERG K⁺ channel inhibition test. Furthermore, its phosphate was found to be highly soluble in water (47.1 mg/mL), which is beneficial for the subsequent in vivo test. In MRSA systemic infection mice models, I phosphate exerted significantly improved survival protection compared with linezolid. The compound also demonstrated high oral bioavailability (F = 99.1%). Moreover, from the results of in vivo toxicol. experiments, I phosphate would be predicted to have less bone marrow suppression. In the experiment, the researchers used many compounds, for example, 3-(1H-Pyrazol-3-yl)pyridine (cas: 45887-08-9Synthetic Route of C8H7N3).

3-(1H-Pyrazol-3-yl)pyridine (cas: 45887-08-9) belongs to pyrazole derivatives. Pyrazole has two ring nitrogen atoms in which N1 is pyrrolic and N2 is pyridine-like. The N1 nitrogen is not reactive but is deprotonated in the presence of a base-forming anion. Protonation of pyrazole in strong acid leads to pyrazolium cations, which undergo electrophilic substitution preferentially at C3 rather than C4. The pyrazole anion is not reactive toward nucleophiles but is mostly reactive to electrophiles.Synthetic Route of C8H7N3

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Substituent-oriented C-N bond formation via N-H insertion or Wolff rearrangement of 5-aryl-1H-pyrazoles and diazo compounds was written by Zuo, Youpeng;He, Xinwei;Ning, Yi;Tang, Qiang;Xie, Mengqing;Hu, Wangcheng;Shang, Yongjia. And the article was included in Organic & Biomolecular Chemistry in 2019.Formula: C9H7BrN2 This article mentions the following:

A facile and efficient synthetic strategy for the chemoselective synthesis of N-substituted 3-aryl-1H-pyrazole derivatives was developed and it was oriented by different 2-diazo compounds Both N-H insertion and Wolff-rearrangement products were obtained selectively by the opportune choice of diazo compounds N-Cyclohexenone 3-aryl-1H-pyrazoles were formed using cyclic 2-diazo-1,3-diketones via N-H insertion in the presence of a copper catalyst and α-carbonyl 3-aryl-1H-pyrazoles were be synthesized through a Wolff-rearrangement process without any catalyst under thermal conditions. Moreover, both reactions were carried out in moderate to excellent yields (58-93%) and showed good functional group tolerance. In the experiment, the researchers used many compounds, for example, 3-(4-Bromophenyl)-1H-pyrazole (cas: 73387-46-9Formula: C9H7BrN2).

3-(4-Bromophenyl)-1H-pyrazole (cas: 73387-46-9) belongs to pyrazole derivatives. Pyrazoles, a five-membered heterocycle containing two adjacent nitrogen atoms, are the core structures found in a number of molecules that possess a wide range of pharmaceutical and agricultural activities. Pyrazoles can be selectively lithiated at different carbons and subsequently react with electrophiles depending on the substitution patterns.Formula: C9H7BrN2

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics