Wen, Shijun et al. published their patent in 2021 |CAS: 882518-89-0

The Article related to heterocyclic small mol compound preparation ezh2 protein antitumor agent, Heterocyclic Compounds (One Hetero Atom): Pyridines and other aspects.Related Products of 882518-89-0

On August 6, 2021, Wen, Shijun; Huang, Peng; Tu, Yalin; Sun, Yameng; Hu, Yumin published a patent.Related Products of 882518-89-0 The title of the patent was Preparation of small molecule compounds based on degradation of EZH2 protein and their applications. And the patent contained the following:

The present invention relates to the preparation of small mol. compounds based on degradation of EZH2 protein and their applications. In particular, the small mol. compound I (wherein, X = a linker including acyclic or cyclic saturated or unsaturated carbon, ethylene glycol, amide, amino, ether, or carbonyl-containing group; Y = can be a group of affinity E3 ligase VHL or Cereblon (CRBN)) was prepared The inventive EZH2 degrading agents that can specifically degrade EZH2 protein, and these small mol. compounds has a stronger anti-tumor effect compared with EZH2 inhibitors. The experimental process involved the reaction of tert-Butyl 2-(2-(2-(tosyloxy)ethoxy)ethoxy)acetate(cas: 882518-89-0).Related Products of 882518-89-0

The Article related to heterocyclic small mol compound preparation ezh2 protein antitumor agent, Heterocyclic Compounds (One Hetero Atom): Pyridines and other aspects.Related Products of 882518-89-0

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

You, Shuli et al. published their patent in 2009 |CAS: 93476-46-1

The Article related to indolizine derivative halogenation, haloindolizine derivative preparation, Heterocyclic Compounds (One Hetero Atom): Pyridines and other aspects.Computed Properties of 93476-46-1

On July 22, 2009, You, Shuli; Xia, Jibao published a patent.Computed Properties of 93476-46-1 The title of the patent was Method for synthesizing 3-haloindolizine. And the patent contained the following:

The invention relates to the method for preparation of 3-haloindolizine derivatives of formula I. Compounds of formula I wherein R1 and R2 are independently H, C1-16 alkyl, C3-16 cycloalkyl, amino and derivatives,C1-16 alkoxy, halo, C1-16 alkanoyl, C5-10 heterocyclyl, C5-10 heteroaryl, etc.; are claimed. Compounds of formula I were prepared via halogenation of indolizines with copper halides. The method has the advantages of broad scope of suitable substrates, low cost, mild reaction conditions, easy operation, high efficiency, and high selectivity. The experimental process involved the reaction of Ethyl indolizine-1-carboxylate(cas: 93476-46-1).Computed Properties of 93476-46-1

The Article related to indolizine derivative halogenation, haloindolizine derivative preparation, Heterocyclic Compounds (One Hetero Atom): Pyridines and other aspects.Computed Properties of 93476-46-1

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Yang, Yuzhu et al. published their research in Organic Letters in 2009 |CAS: 93476-46-1

The Article related to regioselective oxidative coupling indolizine vinylarene palladium catalyst, Heterocyclic Compounds (One Hetero Atom): Pyridines and other aspects.Application of 93476-46-1

On December 17, 2009, Yang, Yuzhu; Cheng, Kai; Zhang, Yuhong published an article.Application of 93476-46-1 The title of the article was Highly Regioselective Palladium-Catalyzed Oxidative Coupling of Indolizines and Vinylarenes via C-H Bond Cleavage. And the article contained the following:

A highly regioselective oxidative coupling reaction between indolizines and vinylarenes has been accomplished in the presence of palladium catalysts to give only the branched α-product in high efficiency. The regioselectivity is promoted significantly by bidentate nitrogen ligands. The experimental process involved the reaction of Ethyl indolizine-1-carboxylate(cas: 93476-46-1).Application of 93476-46-1

The Article related to regioselective oxidative coupling indolizine vinylarene palladium catalyst, Heterocyclic Compounds (One Hetero Atom): Pyridines and other aspects.Application of 93476-46-1

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Gaalova, Jana et al. published their research in Separation and Purification Technology in 2019 |CAS: 3976-69-0

The Article related to pdms membrane methyl hydroxybutyrate pervaporation ionic liquid ru catalyst, Plastics Fabrication and Uses: Plastic Product Uses and other aspects.Quality Control of (R)-Methyl 3-hydroxybutanoate

On September 1, 2019, Gaalova, Jana; Hejda, Stanislav; Stavarek, Petr; Sykora, Jan; Fajgar, Radek; Kluson, Petr; Izak, Pavel published an article.Quality Control of (R)-Methyl 3-hydroxybutanoate The title of the article was Pervaporation of (R)/(S)-methyl 3-hydroxybutyrate (∑MHB) from a mixture containing an ionic liquid, methanol and Ru catalyst. And the article contained the following:

Complex technologies in the production of fine chems. bring together various connected processes, each bringing specific green chem. challenges. A valuable mixture arises in the stereoselective hydrogenation of methyl-acetoacetate (MAA) to (R)- and (S)- Me 3-hydroxybutyrate (∑MHB) over Ru organometallic complex (R)-Ru/BINAP, and in a “green” tetra-alkylammonium bistriflimide/methanol/water solvent phase. The reaction could be carried out in various arrangements, e.g. in a batch mode, in a continuous stirred-tank reactor, or even in a tubular microfluidic chip reactor. In either case, the valuable optically pure Ru complex has been sought to be effectively separated, and potentially recycled. The ionic liquid phase (tetra-alkylammonium bistriflimide) is intended for selective accommodation of the complex in the reaction mixture and as a green alternative to other solvents. It was the main issue of this work to design a specific separation unit, to construct it, and to optimize its performance towards the efficient separation of ∑MHB from the ionic liquid phase bearing the (R)-Ru/BINAP complex. The unit was developed to be connected with the complex preparation process, employing the microreactor fluid flow platform. The separation part of the overall technol. was designed as a membrane pervaporation. The membrane separation proceeded with different feed mixtures combining ∑methyl 3-hydroxybutyrate, methanol, ionic liquid and/or the catalyst. The technique was applied at various temperatures, using the industrial composite PDMS membrane, PERVAP 4060 from Sulzer. The feed as well as the pervaporate were analyzed by NMR spectroscopy and IR spectroscopy. The enrichment factor of the ∑MHB with respect to the retentate was 1.24 and the ∑MHB permeate mass flux was 61 g h-1 m-2. In addition, the membrane was characterized by SEM and energy dispersive X-ray microanal. after the membrane process, showing no sorption of the catalyst into the membrane. The experimental process involved the reaction of (R)-Methyl 3-hydroxybutanoate(cas: 3976-69-0).Quality Control of (R)-Methyl 3-hydroxybutanoate

The Article related to pdms membrane methyl hydroxybutyrate pervaporation ionic liquid ru catalyst, Plastics Fabrication and Uses: Plastic Product Uses and other aspects.Quality Control of (R)-Methyl 3-hydroxybutanoate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Castro Palomino Laria, Julio Cesar et al. published their patent in 2009 |CAS: 141940-37-6

The Article related to azabiphenylaminobenzoic acid preparation dihydroorotate dehydrogenase dhodh inhibitor, Heterocyclic Compounds (One Hetero Atom): Pyridines and other aspects.Recommanded Product: 141940-37-6

On February 19, 2009, Castro Palomino Laria, Julio Cesar; Terricabras Belart, Emma; Erra Sola, Montserrat; Navarro Romero, Eloisa; Fonquerna Pou, Silvia; Cardus Figueras, Aranzazu; Lozoya Toribio, Maria Estrella published a patent.Recommanded Product: 141940-37-6 The title of the patent was Preparation of azabiphenylaminobenzoic acid derivatives as DHODH inhibitors. And the patent contained the following:

The title compounds I [R1 = H, halo, alkyl, etc.; R2 = H, halo, alkyl; R3 = CO2R5, CONHR5, tetrazolyl, SO2NHR5, CONHSO2R5 (wherein R5 = H, alkyl); R4 = H, alkyl; R9 = H, Ph; G1 = N, CR6 (R6 = H, halo, alkyl, etc.); G2 = H, OH, halo, cycloalkyl, etc.], useful as inhibitors of the dihydroorotate dehydrogenase (DHODH), were prepared and formulated. Thus, heating 2-amino-5-cyclopropylbenzoic acid with 5-bromo-2-phenylpyrimidine (preparations given) in the presence of Cu2O, Cu and K2CO3 in DME at 130°C afforded 57% II which showed IC50 of 105 nM against hDHODH. Pharmaceutical compositions comprising I, alone or in combination with other therapeutic agent, were disclosed. The experimental process involved the reaction of tert-Butyl (4-(trifluoromethyl)phenyl)carbamate(cas: 141940-37-6).Recommanded Product: 141940-37-6

The Article related to azabiphenylaminobenzoic acid preparation dihydroorotate dehydrogenase dhodh inhibitor, Heterocyclic Compounds (One Hetero Atom): Pyridines and other aspects.Recommanded Product: 141940-37-6

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Arslan, Gulsin et al. published their research in Desalination and Water Treatment in 2017 |CAS: 3319-31-1

The Article related to polymer inclusion membrane reproducible transport sodium diethyldithiocarbamate zinc ion, Plastics Fabrication and Uses: Plastic Product Uses and other aspects.Formula: C33H54O6

On May 31, 2017, Arslan, Gulsin; Yilmaz, Abdurrahman; Tor, Ali; Ersoz, Mustafa published an article.Formula: C33H54O6 The title of the article was Preparation of polymer inclusion membrane with sodium diethyldithiocarbamate as a carrier reagent for selective transport of zinc ions. And the article contained the following:

This study reports the design of a new type of polymer inclusion membrane (PIM) for selective transport of zinc ion. Sodium diethyldithiocarbamate (NaDDTC) was incorporated in the cellulose acetate-based membrane as a carrier for Zn(II) ion. The PIMs were characterized using Fourier transform IR spectroscopy, SEM, at. force microscopy and contact angle measurements. The effects of parameters, including concentration of Zn(II) in the feed phase, HCl in the stripping phase and amount of NaDDTC incorporated in the membrane, on the transport of Zn(II) ion were studied. For 1×10-4 M of Zn(II) ion in the feed phase at pH 5.04, 96% of Zn(II) ion was transported through the PIMs prepared with 1.0 (wt%) diethyldithiocarbamate via 0.5 M HCl as a stripping phase. The diffusion of Zn(II) ions through the membrane was governed by complex formation between Zn(II) ion and NaDDTC in the membrane. Moreover, selective transport of Zn(II) ion was achieved in the presence of divalent metal ions involving Cu(II), Pb(II) and Ni(II). The prepared PIM provided reproducible transport efficiency, and it can be efficiently used in separation processes. The experimental process involved the reaction of Tris(2-ethylhexyl) benzene-1,2,4-tricarboxylate(cas: 3319-31-1).Formula: C33H54O6

The Article related to polymer inclusion membrane reproducible transport sodium diethyldithiocarbamate zinc ion, Plastics Fabrication and Uses: Plastic Product Uses and other aspects.Formula: C33H54O6

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Amaral, Monica F. Z. J. et al. published their research in Organic Letters in 2015 |CAS: 93476-46-1

The Article related to indolizine regioselective synthesis, electrophile indolizine organometallic base metalation, Heterocyclic Compounds (One Hetero Atom): Pyridines and other aspects.Product Details of 93476-46-1

On January 16, 2015, Amaral, Monica F. Z. J.; Baumgartner, Amanda A.; Vessecchi, Ricardo; Clososki, Giuliano C. published an article.Product Details of 93476-46-1 The title of the article was Directed Metalation of 1-Ester-Substituted Indolizines: Base/Electrophile-Controlled Regioselective Functionalization. And the article contained the following:

A variety of C-2 and C-5 difunctionalized indolizines e. g., I, have been prepared through the reaction of 1-ester-substituted indolizines with organometallic bases followed by a reaction with different electrophiles. Metalation takes place under mild conditions allowing the isolation of a number of difunctionalized indolizines in good yields. The regioselectivity of the reaction appears to be governed by the nature of the base and electrophile. The experimental process involved the reaction of Ethyl indolizine-1-carboxylate(cas: 93476-46-1).Product Details of 93476-46-1

The Article related to indolizine regioselective synthesis, electrophile indolizine organometallic base metalation, Heterocyclic Compounds (One Hetero Atom): Pyridines and other aspects.Product Details of 93476-46-1

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Zhong, Sabilla et al. published their research in RSC Advances in 2015 |CAS: 1414887-27-6

The Article related to perfluoroalkylated arene preparation, arene perfluorocarboxylic anhydride perfluoroalkylation, Aliphatic Compounds: Halides and Halonium Compounds and other aspects.Category: esters-buliding-blocks

Zhong, Sabilla; Hafner, Andreas; Hussal, Christoph; Nieger, Martin; Braese, Stefan published an article in 2015, the title of the article was Metal-free radical perfluoroalkylation of (hetero)arenes.Category: esters-buliding-blocks And the article contains the following content:

A metal-free radical perfluoroalkylation method which used inexpensive and com. available perfluorocarboxylic anhydrides as an easy to use source of perfluoroalkyl radicals was reported. This approach allowed the perfluoroalkylation of different arenes, such as benzene derivatives, furans, thiophenes, and pyrroles, including highly functionalized compounds The experimental process involved the reaction of Ethyl 5-(trifluoromethyl)-1H-pyrrole-2-carboxylate(cas: 1414887-27-6).Category: esters-buliding-blocks

The Article related to perfluoroalkylated arene preparation, arene perfluorocarboxylic anhydride perfluoroalkylation, Aliphatic Compounds: Halides and Halonium Compounds and other aspects.Category: esters-buliding-blocks

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Mikamiyama, Hidenori et al. published their patent in 2010 |CAS: 1206550-93-7

The Article related to tetrahydropyridine dihydropyrrole compound preparation pain calcium channel disorder treatment, Heterocyclic Compounds (One Hetero Atom): Pyridines and other aspects.Application In Synthesis of Ethyl 2-(4-(trifluoromethoxy)phenyl)acetate

On February 4, 2010, Mikamiyama, Hidenori; Ni, Chiyou; Shao, Bin; Tafesse, Laykea published a patent.Application In Synthesis of Ethyl 2-(4-(trifluoromethoxy)phenyl)acetate The title of the patent was Preparation of tetrahydropyridine and dihydropyrrole compounds as calcium channel blockers for treatment of pain and other disorders. And the patent contained the following:

The invention relates to tetrahydropyridinyl and dihydropyrrolyl compounds of formula I (wherein X = CO, CH2, or is part of a bridge; R9 = H or is part of a bridge; Hy = a 6- or 5-membered heteroaromatic ring, or a 5-membered heterocyclic ring; Z = SO2-aryl; SO2-cycloalkenyl, CH2-aryl, etc.; R1 = CN, OH-alkyl, CO2H, etc.; R2 = alkyl, alkenyl, alkynyl, etc.; m = 0-3; n = 0-1) and pharmaceutically acceptable salts, prodrugs, or solvates thereof. The invention is also directed to the use of compounds of formula I to treat a disorder responsive to the blockade of calcium channels, and particularly N-type calcium channels. Compounds of the present invention are especially useful for treating pain. Exemplary methods for synthesizing compounds of the invention were described, e.g., II was prepared by a multi-step synthesis involving the preparation of intermediate N-cyclopropyl-6-(1,2,3,6-tetrahydropyridin-4-yl)picolinamide and subsequent reaction with 4-trifluoromethoxybenzaldehyde to give II. Compounds of the invention were tested as N-type calcium channel (NTCC) blockers, and II demonstrated an IC50 value of 0.03 μM. II was also tested in the calcium mobilization assay for L-type calcium channel (LTCC) blocking activity and it showed an LTCC IC50 value of >20 μM in that assay. The experimental process involved the reaction of Ethyl 2-(4-(trifluoromethoxy)phenyl)acetate(cas: 1206550-93-7).Application In Synthesis of Ethyl 2-(4-(trifluoromethoxy)phenyl)acetate

The Article related to tetrahydropyridine dihydropyrrole compound preparation pain calcium channel disorder treatment, Heterocyclic Compounds (One Hetero Atom): Pyridines and other aspects.Application In Synthesis of Ethyl 2-(4-(trifluoromethoxy)phenyl)acetate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Semeraro, Teresa et al. published their patent in 2016 |CAS: 1198284-94-4

The Article related to bisfluorophenylmethyldiazaspirodecanone preparation human dopamine active transporter inhibitor, Heterocyclic Compounds (One Hetero Atom): Pyridines and other aspects.Category: esters-buliding-blocks

On March 24, 2016, Semeraro, Teresa; Tarsi, Luca; Micheli, Fabrizio; Luker, Tim; Cremonesi, Susanna published a patent.Category: esters-buliding-blocks The title of the patent was Preparation of 2-[bis(4-fluorophenyl)methyl]-2,7-diazaspiro[4.5]decan-10-one derivatives useful as inhibitors of human dopamine active transporter (DAT) protein. And the patent contained the following:

The invention relates to compounds of formula I, and in particular 2-[bis(4-fluorophenyl)methyl]-2,7-diazaspiro[4.5]decan-10-one derivatives and related compounds, method for their preparation and their use as inhibitors of human dopamine active transporter (DAT) protein for the treatment of sexual dysfunction, affective disorders, anxiety, depression, attention deficit hyperactivity disorder (ADHD), obesity, etc. Compounds of formula I, wherein Q is C=NOH, NH, Ncycloalkyl, etc.; X is CO, NH, Nalkyl, etc.; Y is O, SO0-2, Nalkyl, etc.; Z is O, S and CR11R12; A is (CHR5R6)0-2; B is (CR1R2)0-2; M is (R9R10)0-2; R1 and R2 are independently H, OH, F, alkyl, etc., or R1R2 together form =O; R3, R4, R7 and R8 are independently H, OH, alkoxy and alkyl, or R3 and R4, R7 and R8 may both be O, wherein said O atoms are linked by an alkylene group to form a straight chain or branched alkylenedioxy group; R5 and R6 are independently H and alkyl, or R5 and R6 from =O; R13 is substituted phenyl; R14 is (un)substituted phenyl; R9, R10, R11 and R12 are independently H and alkyl, are claimed. Example compound II was prepared by a multistep procedure (procedure given). All the invention compounds were evaluated for their affinity to the human transporters DAT, NET, SERT and hERG. From the assay, it was determined that example compound II exhibited pIC50 value of 6.89, 5.42, 4.65 and 5.7 towards human transporters DAT, NET, SERT and hERG resp. The experimental process involved the reaction of tert-Butyl 1-oxo-2,9-diazaspiro[5.5]undecane-9-carboxylate(cas: 1198284-94-4).Category: esters-buliding-blocks

The Article related to bisfluorophenylmethyldiazaspirodecanone preparation human dopamine active transporter inhibitor, Heterocyclic Compounds (One Hetero Atom): Pyridines and other aspects.Category: esters-buliding-blocks

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics