The Dimroth rearrangement in the synthesis of condensed pyrimidines–structural analogs of antiviral compounds

VА Mamedov, NА Zhukova, MS Kadyrova - Chemistry of Heterocyclic …, 2021 - Springer
The Dimroth Rearrangement in the Synthesis of Condensed Pyrimidines – Structural
Analogs of Antiviral Compounds | SpringerLink Skip to main content Advertisement …

Azo-coupling of pyrazole-3 (5)-diazonium chlorides with cyanothioacetamide: a convenient synthesis of pyrazolo [5, 1-c][1, 2, 4] triazine-3-carbothioamides

IV Ledenyova, VV Didenko, VV Dotsenko… - Tetrahedron …, 2014 - Elsevier
Abstract Cyanothioacetamide reacts with pyrazole-3 (5)-diazonium chlorides to afford
pyrazolo [5, 1-c][1, 2, 4] triazine-3-carbothioamides 5. The latter can be oxidized with H 2 O 2 …

Synthesis of New Azocompounds and Fused Pyrazolo[5,1‐c][1,2,4]triazines Using Heterocyclic Components

IV Ledenyova, VV Didenko… - Journal of …, 2013 - Wiley Online Library
Diazotization of 3‐methyl‐4‐phenyl‐1H‐pyrazol‐5‐amine 1 in hydrochloric acid has been
reported to afford the corresponding diazonium salt 2. The latter underwent azocoupling with …

Polycyclic N-heterocyclic compounds. Part 58: Rearrangement reactions of fused 3-(2-bromoethyl) pyrimidin-4 (3H)-ones with primary amines and antidepressive …

H Ohtomo, T Tagata, K Sasaki, T Hirota, K Okuda - Tetrahedron, 2007 - Elsevier
Reaction of fused 3-(2-bromoethyl) pyrimidin-4 (3H)-ones with primary alkylamines gave
abnormal fused 3-alkyl-4-alkyliminopyrimidines via a new rearrangement, as well as normal …

A Convenient Approach to 4,7‐Dihydrotetrazolo [5,1‐c][1,2,4]triazine Synthesis

EV Shchegol'kov, AE Ivanova… - Journal of …, 2013 - Wiley Online Library
Azo coupling of 1, 3‐dicarbonyl compounds with tetrazolyl‐5‐diazonium chloride is used to
develop a convenient one‐step procedure for the synthesis of 4, 7‐dihydrotetrazolo [5, 1 …

Controlled Dimroth Rearrangement in the Suzuki–Miyaura Cross Coupling of Triazolopyridopyrimidines

A Champiré, C Vala, A Laabid… - The Journal of …, 2016 - ACS Publications
Polynitrogen heterocycles are often subject to Dimroth rearrangement which consists of ring
opening, bond rotation, and ring closure. In this note, we report a synthesis of two new …

Novel triazinium-imidothioate zwitterions: intermediates in the reaction of [1, 3, 4] thiadiazolo [2, 3-d][1, 2, 4] triazolo [1, 5-a][1, 3, 5] triazinium cations with amines

K Wermann, M Walther, W Günther, H Görls, E Anders - Tetrahedron, 2005 - Elsevier
Starting with bis ([1, 3, 4] thiadiazolo)[1, 3, 5] triazinium halides, a novel class of heterocyclic
compounds, the [1, 3, 4] thiadiazolo [2, 3-d][1, 2, 4] triazolo [1, 5-a][1, 3, 5] triazinium halides …

Mixed oxides as highly selective catalysts for the flash pyrolysis of phenacyl benzotriazole: one-pot synthesis of dibenzazepin-7-one

G Lener, RE Carbonio, EL Moyano - ACS Catalysis, 2013 - ACS Publications
The one-pot synthesis of dibenzo [b, d] azepin-7-one (3) was selectively achieved from 1-
phenacyl-1, 2, 3-benzotriazole (1) using the catalytic flash vacuum pyrolysis (cfvp) …

Unexpected ANRORC rearrangement in pyran ring

VV Kurdyukov, IV Kurdyukova - Chemistry of Heterocyclic Compounds, 2022 - Springer
Unexpected ANRORC rearrangement in pyran ring | Chemistry of Heterocyclic Compounds
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Synthesis of diheteroaryl sulfides via chemoselective reaction of 4,6-diaminopyrimidine-2(1H)-thione with haloheteroaryl compounds

T Davodian, R Ranjbar-Karimi, H Mehrabi - Chemistry of Heterocyclic …, 2017 - Springer
A series of substituted diheteroaryl sulfides was synthesized by the reaction of 4, 6-
diaminopyrimidine-2 (1 H)-thione with fluoro-and chloroheteroaromatic compounds in the …