Relevant bibliographies by topics / Pyridine(bromo-3 methoxy-2)

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Academic literature on the topic 'Pyridine(bromo-3 methoxy-2)'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 February 2022

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Journal articles on the topic "Pyridine(bromo-3 methoxy-2)"

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Sowmya, Haliwana B. V., Tholappanavara H. Suresha Kumara, Nagendrappa Gopalpur та ін. "Crystal structures of five (2-chloroquinolin-3-yl)methyl ethers: supramolecular assembly in one and two dimensions mediated by hydrogen bonding and π–π stacking". Acta Crystallographica Section E Crystallographic Communications 71, № 6 (2015): 609–17. http://dx.doi.org/10.1107/s2056989015008233.

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In the molecules of the title compounds, methyl 5-bromo-2-[(2-chloroquinolin-3-yl)methoxy]benzoate, C18H13BrClNO3, (I), methyl 5-bromo-2-[(2-chloro-6-methylquinolin-3-yl)methoxy]benzoate, C19H15BrClNO3, (II), methyl 2-[(2-chloro-6-methylquinolin-3-yl)methoxy]benzoate, C19H16ClNO3, (III), which crystallizes withZ′ = 4 in space groupP212121, and 2-chloro-3-[(naphthalen-1-yloxy)methyl]quinoline, C20H14ClNO, (IV), the non-H atoms are nearly coplanar, but in {5-[(2-chloroquinolin-3-yl)methoxy]-4-(hydroxymethyl)-6-methylpyridin-3-yl}methanol, C18H17ClN2O3, (V), the planes of the quinoline unit and o
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2

Zhang, Ji-Run, Hao Deng, and Tong Liu. "The crystal structure of 3-bromo-6-methoxy-2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, C13H19BBrNO3." Zeitschrift für Kristallographie - New Crystal Structures 235, no. 2 (2020): 451–52. http://dx.doi.org/10.1515/ncrs-2019-0756.

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AbstractC13H19BBrNO3, triclinic, P1̄ (no. 2), a = 6.5459(3) Å, b = 11.2565(5) Å, c = 11.8529(5) Å, α = 106.938(2)°, β = 105.657(2)°, γ = 106.628(2)°, V = 738.71(6) Å3, Z = 2, Rgt(F) = 0.0286, wRref(F2) = 0.0641, T = 173 K.
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Çolak, N., A. Karayel, K. Buldurun, and N. Turan. "SYNTHESIS, CHARACTERIZATION, THERMAL, X-RAY, AND DFT ANALYSES OF 6-TERT-BUTYL 3-ETHYL 2-[(3-METHOXY/5-BROMO)-2-HYDROXY AND (3-NITRO/3-METHOXY)BENZYLIDENEAMINO]- 4,5-DIHYDROTHIENO[2,3-C]PYRIDINE-3,6(7H)-DICARBOXYLATE." Journal of Structural Chemistry 62, no. 1 (2021): 37–46. http://dx.doi.org/10.1134/s0022476621010054.

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Jindřich, Jindřich, Hana Dvořáková, and Antonín Holý. "Synthesis of Isomeric N-(3-Fluoro-2-hydroxypropyl) and N-(2-Fluoro-3-hydroxypropyl) Derivatives of Purine and Pyrimidine Bases." Collection of Czechoslovak Chemical Communications 57, no. 7 (1992): 1466–82. http://dx.doi.org/10.1135/cccc19921466.

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Reaction of fluoromethyloxirane (III) with heterocyclic bases in the presence of potassium carbonate afforded N-(3-fluoro-2-hydroxypropyl) derivatives of adenine (VI), 3-deazaadenine (VII), 2-amino-6-chloropurine (XII), 6-nitro-1-deazapurine (IX), 4-methoxy-2-pyrimidone (XVIII) and its 5-methyl derivative (XIX). Acid hydrolysis of compounds XII, XVIII, and XIX gave 9-(3-fluoro-2-hydroxypropyl)guanine (XIII), 1-(3-fluoro-2-hydroxypropyl)uracil (XX) and -thymine (XXI). The intermediates XVIII and XIX were ammonolyzed to give 1-(3-fluoro-2-hydroxypropyl)cytosine (XXII) and -5-methylcytosine (XXII
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Sihver, Wiebke, Karl-Johan Fasth, Andrew G. Horti, et al. "Synthesis and Characterization of Binding of 5-[76Br] Bromo-3-[[2(S)-Azetidinyl]methoxy]pyridine, a Novel Nicotinic Acetylcholine Receptor Ligand, in Rat Brain." Journal of Neurochemistry 73, no. 3 (2001): 1264–72. http://dx.doi.org/10.1046/j.1471-4159.1999.0731264.x.

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Barlin, GB, LP Davies, PW Harrison, NW Jacobsen, and AC Willis. "Imidazo[1,2-b]Pyridazines. XVI. Synthesis and Central Nervous System Activities of Some 6-(Chloro, Alkylthio, Phenylthio, Benzylthio or Pyridinylmethylthio)-3-(unsubstituted, benzamidomethyl or methoxy)-2-(styryl or benzoyl)imidazo[1,2-b]pyridazines." Australian Journal of Chemistry 47, no. 11 (1994): 1989. http://dx.doi.org/10.1071/ch9941989.

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Some 6-( chloro, alkylthio, phenylthio, benzylthio or pyridinylmethylthio )-3-( unsubstituted , benzamidomethyl or methoxy )-2-styrylimidazo[1,2-b] pyridazines and 6-chloro-3-( unsubstituted and benzamidomethyl )-2-benzoylimidazo[1,2-b] pyridazines have been prepared and tested for their ability to displace [3H]diazepam from rat brain plasma membranes. The structures of 6-chloro-2-benzoyl[and 6-fluoro-2-(4′-tolyl)] imidazo [1,2-b] pyridazine have been confirmed by X-ray analyses. The reactions of 6-methylthio(and 6-phenylthio)pyridazin-3-amines with 3-bromo-1-phenylpropane-1,2-dione also have
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7

Reddy, B. Siva, and K. R. S. Prasad. "Design, Synthesis and Antibacterial Activity of N-(3-((4-(6-(2,2,2- Trifluoroethoxy)pyridin-3-yl)-1H-imidazol-2-yl)methyl)oxetan-3-yl)amide Derivatives." Asian Journal of Chemistry 33, no. 3 (2021): 577–82. http://dx.doi.org/10.14233/ajchem.2021.23039.

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A new series of N-(3-((4-(6-(2,2,2-trifluoroethoxy)pyridin-3-yl)-1H-imidazol-2-yl)methyl)oxetan-3- yl)amide derivatives (10a-h)were synthesized by the reaction of 3-((4-(6-(2,2,2-trifluoroethoxy)pyridin- 3-yl)-1H-imidazol-2-yl)methyl)oxetan-3-amine (8) with various carboxylic acids in the presence of T3P catalyst. The reaction is usually furnished within 60 min with good isolated yields. Coupling of 6-(2,2,2-trifluoroethoxy) nicotinic acid (1) with Weinreb amine hydrochloride gave N-methoxy-Nmethyl- 6-(2,2,2-trifluoroethoxy) nicotinamide (2). Compound 3 was synthesized by the Grignard reaction
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8

"Synthesis, Characterization, Thermal, X-ray and DFT Analysis of 6-tert-butyl 3-ethyl 2-[(3-methoxy/5-bromo)-2-hydroxy and (3-nitro/3-methoxy)benzylideneamino]-4,5-dihydrothieno[2,3-c]pyridine-3,6(7H)-dicarboxylate." Журнал структурной химии 62, no. 2 (2021). http://dx.doi.org/10.26902/jsc_id68309.

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Dissertations / Theses on the topic "Pyridine(bromo-3 methoxy-2)"

1

Trécourt, François. "Elaboration de dérivés carbonylés orthosubstitués de la pyridine : application d'une nouvelle méthode de synthèse de pyridines, synthèse d'hétérocycles du type coumarine et xanthone." Rouen, 1987. http://www.theses.fr/1987ROUES021.

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A partir de bromo-3 pyridines orthosubstituées par un fluor, un chlore, un méthoxy, un méthylthio, une première méthode de synthèse a permis d'élaborer des dérivés carbonylés (aldéhydes, cétones) orthosubstitués de la pyridine en utilisant la réaction d'échange halogène-métal. Cette méthode donne de bons résultats mais comporte en général un nombre important d'étapes. Une deuxième méthode de synthèse des dérivés carbonylés orthosubstitués de la pyridine a été mise en oeuvre. Cette méthode, basée sur la réaction de métallation régiosélective de dérivés monosubstitués de la pyridine (fluoro, chl
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