Results 31 to 40 of about 1,673 (99)

Synthesis of N‑Aryl-3,5-dichloro‑4H‑1,2,6-thiadiazin-4-imines from 3,4,4,5-Tetrachloro‑4H‑1,2,6-thiadiazine

open access: yes, 2015
Condensation of 3,4,4,5-tetrachloro-4H-1,2,6-thiadiazine with a range of anilines gave 22 N-aryl-3,5-dichloro-4H-1,2,6-thiadiazin-4-imines in 43–96% yields. The scope and limitations of this condensation are briefly investigated.
Maria Manoli (1339620)   +2 more
core   +1 more source

Novel bronchodilators: Synthesis, transamination reactions, and pharmacology of a series of pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides

open access: yes, 2000
The synthesis, pharmacological evaluation, and structure-activity relationships of a new class of bronchodilator agents, derivatives of pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides are described.
Alkorta, Ibon   +10 more
core   +1 more source

Synthesis of 3-[(2-Ethylhexyl)amino]-5-phenyl-4H-1,2,6-thiadiazin-4-one and 3-[(2-Ethylhexyl)amino]-5-[(4-oxo-5-phenyl-4H-1,2,6-thiadiazin-3-yl)amino]-4H-1,2,6-thiadiazin-4-one

open access: yesMolbank
Suzuki–Miyaura coupling of 3-chloro-5-[(2-ethylhexyl)amino]-4H-1,2,6-thiadiazin-4-one with phenylboronic acid, at ca. 100 °C, gave 3-[(2-ethylhexyl)amino]-5-phenyl-4H-1,2,6-thiadiazin-4-one in 69% yield.
Andreas S. Kalogirou   +1 more
doaj   +1 more source

Synthesis of Oligomeric 4H‐1,2,6‐Thiadiazines

open access: yesChemistrySelect, Volume 10, Issue 7, February 19, 2025.
The study reports the synthesis of oligomeric amino‐4H‐1,2,6‐thiadiazines that were efficiently obtained in high yields through C─N coupling reactions. Three analogs with terminal phenyl groups, containing up to four thiadiazine units, were prepared, as well as two amino‐substituted bisthiadiazine oligomers.
Andreas S. Kalogirou   +2 more
wiley   +1 more source

Novel Bronchodilators:  Synthesis, Transamination Reactions, and Pharmacology of a Series of Pyrazino[2,3-c][1,2,6]thiadiazine 2,2-Dioxides

open access: yes, 2016
The synthesis, pharmacological evaluation, and structure−activity relationships of a new class of bronchodilator agents, derivatives of pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides are described.
Concepción García (363008)   +4 more
core   +1 more source

Entwicklung der Synthesen von N-Heterozyklen, Sulfonimidamiden und einem [$^{125}I$]-markierten PARP-Inhibitor

open access: yes, 2022
The content of this work is the synthesis of trifluoroethylated 5- and 6-membered N heterocycles by radical trifluoromethylation of vinyl azides. Furthermore, sulfonimidoyl chlorides and their reaction with pyridium N oxides were studied.
Terhorst, Steven
core   +1 more source

5-Cyano-7-(2-hydroxyphenyl)-4-[(2-hydroxyphenyl)amino]pyrrolo[2,3-c][1,2,6]thiadiazin-6(7H)-iminium Chloride Hydrate

open access: yesMolbank
Reaction of 2-(3,5-dichloro-4H-1,2,6-thiadiazin-4-ylidene)malononitrile with sodium 2-aminophenolate (1.5 equiv.) in anhydrous THF at ca. 0–20 °C afforded the known 4-chlorobenzo[5,6][1,4]oxazino[2,3-c][1,2,6]thiadiazine in 76% yield.
Andreas S. Kalogirou   +2 more
doaj   +1 more source

Discovery of 1,1-dioxo-1,2,6-thiadiazine-5-carboxamide derivatives as cannabinoid-like molecules with agonist and antagonist activity

open access: yes, 2007
A series of new 2-substituted 1,1-dioxo-1,2,6-thiadiazine-5-carboxylate derivatives have been prepared from monosubstituted sulfamides in order to obtain N-substituted 1,1-dioxo-1,2,6-thiadiazine-5-carboxamides as novel cannabinoid derivatives ...
Cano, Carolina   +5 more
core   +1 more source

On the reactivity of 1H-pyrazino[2,3-c] [1,2,6]thiadiazine 2,2-dioxide and derivatives: Nucleophilic substitution, amination, aldol-type condensation, oxidation, and hydrolysis

open access: yes, 2013
The reactivity of the 1H-pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxide system, structurally related to pteridine, was studied, and a number of novel derivatives were synthesized.
Goya, Pilar   +2 more
core   +1 more source

A study of peculiar tautomerism of pyrido[2,3-c][1,2,6]thiadiazine 2,2-dioxide system

open access: yes, 2013
A systematic study of the tautomerism of 4-amino-1H-pyrido[2,3-c][1,2,6] thiadiazine 2,2-dioxide has been carried out. Thus, the relativity stability of the possible tautomers has been studied in the gas phase by ab initio and functional density theory ...
Montero, C.   +2 more
core   +1 more source

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