Tag: M.W=100-150

Zhang, Tao; Luan, Yu-Xin; Lam, Nelson Y. S.; Li, Jiang-Fei; Li, Yue; Ye, Mengchun; Yu, Jin-Quan published the artcile< A directive Ni catalyst overrides conventional site selectivity in pyridine C-H alkenylation>, Category: ethers-buliding-blocks, the main research area is alkenylated pyridine preparation; alkyne pyridine alkenylation heterocyclic carbene ligated nickel aluminum catalyst.

Herein, application of bifunctional N-heterocyclic carbene-ligated Ni-Al catalyst in C3-H alkenylation of pyridines was described. This method overrode the intrinsic C2 and/or C4 selectivity, and provided a series of C3-alkenylated pyridines such as I in 43-99% yields and up to 98:2 C3 selectivity. This method not only allowed a variety of pyridine and heteroarene substrates to be used as the limiting reagent, but was also effective for the late-stage C3 alkenylation of diverse complex pyridine motifs in bioactive mols.

Nature Chemistry published new progress about Alcohols Role: RCT (Reactant), RACT (Reactant or Reagent). 6482-24-2 belongs to class ethers-buliding-blocks, and the molecular formula is C3H7BrO, Category: ethers-buliding-blocks.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Yoon, Hyunjee; Shin, Seoyoon; Park, Sooyeol; Shin, Moo Whan published the artcile< Low-viscosity quaternary ammonium-based ionic liquid electrolytes for lithium air batteries>, Category: ethers-buliding-blocks, the main research area is ammonium ionic liquid electrolyte lithium air battery viscosity.

Ionic liquids (ILs) have attracted significant attention as candidates for Li-air battery electrolyte solvents owing to their novel properties, such as non-volatility and low reactivity with lithium metal anodes. However, the main drawback of IL-based electrolytes is their high viscosity, which results in poor battery capacity and conductivity In this study, we synthesized low-viscosity ILs with reduced mol. weights using the side-chain shortening method. In particular, the IL: tri-Me ethoxymethyl ammonium bis(fluoromethylsulfonyl)imide (N111(1O2) FSI), has a lower viscosity (111.4 cP) than that of the electrochem. stable reference material, diethylmethyl (2-methoxyethyl) ammonium bis(fluoromethylsulfonyl)imide (DEME FSI; viscosity of 131.1cP). The use of the optimal IL, N111(1O2) FSI, resulted in an initial capacity 3.75 times higher than that obtained using DEME FSI in the cell test. The chem. stability of N111(1O2) FSI with lithium metal was confirmed by microstructure anal. of the lithium surface. The physicochem. properties, such as viscosity, ionic conductivity, m.p., and electrochem. properties, were thoroughly characterized.

Journal of Molecular Liquids published new progress about Electric current-potential relationship. 6482-24-2 belongs to class ethers-buliding-blocks, and the molecular formula is C3H7BrO, Category: ethers-buliding-blocks.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Chen, Yuan; Chen, Yu-Jue; Guan, Zhi; He, Yan-Hong published the artcile< Visible-light-mediated selective thiocyanation/ipso-cyclization/oxidation cascade for the synthesis of thiocyanato-containing azaspirotrienediones>, Formula: C8H11NO, the main research area is thiocyanatoazaspirotrienedione preparation; Nphenylpropynamide ammonium thiocyanate thiocyanation ipso cyclization oxidation.

A visible-light-mediated metal-free thiocyanate radical addition/ipso-cyclization/oxidation cascade reaction for the synthesis of thiocyanato-containing azaspirotrienediones from N-phenylpropynamides is described. Cheap and readily available ammonium thiocyanate was used as a precursor to the thiocyanate free radical, which undergoes a radical addition reaction with the alkyne, followed by selective ipso-cyclization and oxidation to afford the dearomatized products. No product of ortho-cyclization was detected. The reaction completes the synthesis of C-S, C-C, and C=O bonds in one pot, with abundant and renewable air oxygen as the sole sacrificial reagent and oxygen source.

Tetrahedron published new progress about Aralkyl amines Role: RCT (Reactant), RACT (Reactant or Reagent). 10541-78-3 belongs to class ethers-buliding-blocks, and the molecular formula is C8H11NO, Formula: C8H11NO.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Chakrabarti, Kaushik; Dutta, Kuheli; Kundu, Sabuj published the artcile< Synthesis of N-methylated amines from acyl azides using methanol>, Safety of 2-Methoxy-N-methylaniline, the main research area is methylated amine preparation acyl azide methanol Curtius rearrangement.

The transformation of acyl azide derivatives into N-methylamines was developed using methanol as the C1 source via the one-pot Curtius rearrangement and borrowing hydrogen methodol. Following this protocol, various functionalized N-methylated amines were synthesized using the (NNN)Ru(II) complex from carboxylic acids via an acyl azide intermediate. Several kinetic studies and DFT calculations were carried out to support the mechanism and also to determine the role of the Ru(II) complex and base in this transformation.

Organic & Biomolecular Chemistry published new progress about Acyl azides Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 10541-78-3 belongs to class ethers-buliding-blocks, and the molecular formula is C8H11NO, Safety of 2-Methoxy-N-methylaniline.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Zhou, Jianmin; Ma, Zhi-Yuan; Shonhe, Chantale; Ji, Su-Hui; Cai, Yun-Rui published the artcile< TEMPO-catalyzed electrochemical dehydrogenative cyclocondensation of o-aminophenols: synthesis of aminophenoxazinones as antiproliferative agents>, Synthetic Route of 40925-69-7, the main research area is aminophenol TEMPO catalyst electrochem dehydrogenative cyclocondensation green chem; aminophenoxazinone preparation antitumor SAR.

A TEMPO-catalyzed electrosynthetic method allowing the dehydrogenative cyclocondensation of o-aminophenols was reported. This mild and sustainable method proceeded in the absence of stoichiometric oxidants and used an easily available organo-electrocatalyst to access pharmaceutically valuable 2-aminophenoxazinones. Mechanistic studies indicated that the electrochem. generated TEMPO+ enables the oxidative radical homo-dimerization of o-aminophenols. The application of electrosynthesis provides an approach for the synthesis of pseudo-aminophenoxazinone alkaloids with improved structural diversification and bioactivities.

Green Chemistry published new progress about Amino phenols Role: PRP (Properties), RCT (Reactant), RACT (Reactant or Reagent). 40925-69-7 belongs to class ethers-buliding-blocks, and the molecular formula is C7H9NO2, Synthetic Route of 40925-69-7.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Guo, Yunhang; Liu, Ye; Hu, Nan; Yu, Desheng; Zhou, Changyou; Shi, Gongyin; Zhang, Bo; Wei, Min; Liu, Junhua; Luo, Lusong; Tang, Zhiyu; Song, Huipeng; Guo, Yin; Liu, Xuesong; Su, Dan; Zhang, Shuo; Song, Xiaomin; Zhou, Xing; Hong, Yuan; Chen, Shuaishuai; Cheng, Zhenzhen; Young, Steve; Wei, Qiang; Wang, Haisheng; Wang, Qiuwen; Lv, Lei; Wang, Fan; Xu, Haipeng; Sun, Hanzi; Xing, Haimei; Li, Na; Zhang, Wei; Wang, Zhongbo; Liu, Guodong; Sun, Zhijian; Zhou, Dongping; Li, Wei; Liu, Libin; Wang, Lai; Wang, Zhiwei published the artcile< Discovery of Zanubrutinib (BGB-3111), a Novel, Potent, and Selective Covalent Inhibitor of Bruton's Tyrosine Kinase>, Electric Literature of 6482-24-2, the main research area is Zanubrutinib BGB3111 Bruton tyrosine kinase inhibitor antitumor.

Aberrant activation of Bruton’s tyrosine kinase (BTK) plays an important role in pathogenesis of B-cell lymphomas, suggesting that inhibition of BTK is useful in the treatment of hematol. malignancies. The discovery of a more selective on-target covalent BTK inhibitor is of high value. Herein, we disclose the discovery and preclin. characterization of a potent, selective, and irreversible BTK inhibitor as our clin. candidate by using in vitro potency, selectivity, pharmacokinetics (PK), and in vivo pharmacodynamic for prioritizing compounds Compound BGB-3111 (31a, Zanubrutinib) demonstrates (i) potent activity against BTK and excellent selectivity over other TEC, EGFR and Src family kinases, (ii) desirable ADME, excellent in vivo pharmacodynamic in mice and efficacy in OCI-LY10 xenograft models.

Journal of Medicinal Chemistry published new progress about B-cell lymphoma. 6482-24-2 belongs to class ethers-buliding-blocks, and the molecular formula is C3H7BrO, Electric Literature of 6482-24-2.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Eeda, Venkateswararao; Awasthi, Vibhudutta published the artcile< Catalyst-Free and Scalable Process for Synthesis of Novel MAP4K4 Inhibitor DMX-5804 and Its Glyco-Conjugates>, Application of C3H7BrO, the main research area is MAP4K4 inhibitor DMX 5804 glyco conjugate preparation.

Here, the process development of scalable and practical synthesis of DMX-5804 I was reported. Process optimization resulted in the following, removal of transition metals from the process and reduced duration of reactions, a streamlined process with significantly improved yields using low-cost raw materials, importantly, microwave-assisted reactions were removed, column purification avoided throughout the process, and crystallized products showed over 95% purity in each step.

Organic Process Research & Development published new progress about Pyrrolopyrimidines Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 6482-24-2 belongs to class ethers-buliding-blocks, and the molecular formula is C3H7BrO, Application of C3H7BrO.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Josse, Pierre; Allain, Magali; Calupitan, Jan Patrick; Jiang, Yue; Cabanetos, Clement; Roncali, Jean published the artcile< Structural Control of the Molecular Packing and Dynamics of Mechanofluorochromic Materials Based on Small Donor-Acceptor Systems with Turn-On Luminescence>, Quality Control of 6482-24-2, the main research area is mechanofluorochromic mol packing luminescence density functional theory.

A series of simple donor-acceptor mols. consisting of an oligo-oxyethylene (OOE) N-substituted diphenylamine connected to a dicyanovinyl (DCV) acceptor group by a thienyl π-conjugating spacer are synthesized. Amorphous deep-red freshly cast thin films rapidly evolve towards an almost colorless pale beige poly-crystalline stable material from which a deep-red photoluminescent state can be switched-on by mech. stimulation. The effects of the length of the OOE chain on the mol. packing of the material and on the dynamics of the recovery process and aggregation in solution are analyzed. Crystallog. results show that the length of the OOE chain directly controls the mol. packing from head-to-tail arrangement of the dipoles for short chain to co-facial dimers leading to a non-centrosym. material with nonlinear optics (NLO) activity for the longer ones. The anal. of the dynamics of the self-recovery process of thin films and of mol. aggregation in solution shows that the dynamics of both processes is directly controlled by the length of the OOE chain. Since, as confirmed by optical and electrochem. results, the OOE substituents have strictly no influence on the electronic properties of the π-conjugated system, the observed effects are unambiguously related to changes in intermol. interactions.

Advanced Optical Materials published new progress about Aldehydes Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 6482-24-2 belongs to class ethers-buliding-blocks, and the molecular formula is C3H7BrO, Quality Control of 6482-24-2.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Yi, Xuewen; Lei, Siyu; Liu, Wangsheng; Che, Fengrui; Yu, Chunzheng; Liu, Xuesong; Wang, Zonghua; Zhou, Xin; Zhang, Yuexia published the artcile< Copper-Catalyzed Radical N-Demethylation of Amides Using N-Fluorobenzenesulfonimide as an Oxidant>, Recommanded Product: 2-Methoxy-N-methylaniline, the main research area is copper catalyzed radical demethylation amide fluorobenzenesulfonimide.

An unprecedented N-demethylation of N-Me amides has been developed by use of N-fluorobenzenesulfonimide as an oxidant with the aid of a copper catalyst. The conversion of amides to carbinolamines involves successive single-electron transfer, hydrogen-atom transfer, and hydrolysis, and is accompanied by formation of N-(phenylsulfonyl)benzenesulfonamide. Carbinolamines spontaneously decompose to N-demethylated amides and formaldehyde, because of their inherent instability.

Organic Letters published new progress about Amides Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation) (N-Me). 10541-78-3 belongs to class ethers-buliding-blocks, and the molecular formula is C8H11NO, Recommanded Product: 2-Methoxy-N-methylaniline.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Xing, Nannan; Niu, Kaixuan; Liu, Kefeng; Fang, Dawei; Ma, Xiaoxue; Guan, Wei; Yang, Jiazhen published the artcile< The molar surface quasi-Gibbs energy and its application to the binary mixtures of 1-(2-methoxyethyl)-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]imide [MOEMIM][NTf2] with methanol and ethanol>, Category: ethers-buliding-blocks, the main research area is molar surface Gibbs energy sulfonylimide methanol ethanol binary mixture.

The IL (ionic liquid) 1-(2-methoxyethyl)-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]imide [MOEMIM][NTf2] was prepared and confirmed by 1H NMR (1H NMR) spectroscopy and 13C NMR (13C NMR) spectroscopy. The d. and surface tension for the binary mixtures of [MOEMIM][NTf2] with methanol and ethanol were measured across the entire range of mole fraction (x1 = 0.0000-1.0000) at T = (288.15-318.15) K. The average molar volumes of the binary mixtures were calculated from the exptl. d., which increased with the increase of mole fraction and temperature The excess molar volumes, VEm, were obtained and fitted by Redlich-Kister equation. The interaction between ionic liquid and alc. is the strongest efficient packing and/or attractive interaction at the min. point. The lower the temperature was, the smaller the absolute value of excess molar volume was. The new function – the molar surface quasi-Gibbs energy of mixtures was obtained by us in this work. On a basis of molar surface quasi-Gibbs energy of mixtures, a new Eotvos equation was obtained of mixtures and applied to binary mixtures of [MOEMIM][NTf2] with alcs. The absolute value of the slope of the new Eotvos equation is the mole surface entropy, s, and the intercept is the molar surface enthalpy, h, which is temperature-independent. The deviation of molar surface quasi-Gibbs energy, Δgs, of mixtures for [MOEMIM][NTf2] with methanol and ethanol were calculated Δgs was well fitted by Redlich-Kister equation. In terms of Redlich-Kisters parameters, Ai, a new method for estimating the surface tension, γ, with any component of the mixtures is proposed and the estimated values, γ (estimate), are in good agreement with the corresponding exptl. ones, γ(exp.).

Journal of Chemical Thermodynamics published new progress about Binary mixtures, liquid. 6482-24-2 belongs to class ethers-buliding-blocks, and the molecular formula is C3H7BrO, Category: ethers-buliding-blocks.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem