Studies with arylhydrazonopyridinones: Synthesis of new arylhydrazono thieno[3,4-c]pyridinones as novel D2T2 dye class; classical verse green methodologies

被引：19

作者：

Al-Zaydi, Khadijah M. ^{[1
]}

Borik, Rita M. ^{[1
]}

Elnagdi, Mohamed H. ^{[2
]}

机构：

[1] Girls Coll Educ, Dept Chem, Jeddah 21533, Saudi Arabia

[2] Kuwait Univ, Fac Sci, Dept Chem, Kuwait 13060, Saudi Arabia

来源：

ULTRASONICS SONOCHEMISTRY | 2009年 / 16卷 / 05期

关键词：

Green chemistry; Microwave irradiation; Ultrasound irradiation; Arylhydrazonopyridinones; Arylhydrazonothieno[3,4-c]pyridinones; X-ray crystal structure determination; HETEROCYCLIC SYNTHESIS; BUILDING-BLOCKS; CHEMISTRY; ULTRASOUND; ROUTE;

D O I：

10.1016/j.ultsonch.2008.11.004

中图分类号：

O42 [声学];

学科分类号：

070206 ; 082403 ;

摘要：

A variety of arylhydrazonopyridinones were prepared via heating cyanoacetamides with ethyl acetoacetate in absence of solvent under reflux conventionally or ultrasound irradiation or in a microwave oven. The formed products 5 and 6 could be readily converted to thienopyridones. Attempted addition of the latter to electron poor olefins afforded only arylhydrazonopyridinones. (C) 2008 Elsevier B.V. All rights reserved.

引用

页码：660 / 668

页数：9

共 42 条

[11] CHEMISTRY OF THE PYRROLO[3,4-C]PYRIDO[2,3-D]PYRIMIDINE SYSTEM - SYNTHESIS OF 6,7-DIHYDROPYRROLO[3,4-C]PYRIDO[2,3-D]PYRIMIDINES, A NOVEL RING-SYSTEM WITH POTENTIAL BIOLOGICAL INTEREST
SU, TL
WATANABE, KA
JOURNAL OF ORGANIC CHEMISTRY, 1989, 54 (01): : 220 - 224
[12] Synthesis, characterization and in vitro antimicrobial activity of novel fused pyrazolo[3,4-c] pyridazine, pyrazolo[3,4-d] pyrimidine, thieno[3,2-c] pyrazole and pyrazolo[3′,4′:4,5]thieno[2,3-d]pyrimidine derivatives (vol 11, 112, 2017)
Reheim, Mohamed A. M. Abdel
Baker, Safaa M.
CHEMISTRY CENTRAL JOURNAL, 2017, 11
[13] Synthesis and characterization of some new thieno[2,3-b]pyridines, b ]pyridines, thieno[2,3c ][2,7]naphthyridinones and pyrazolo[3,4-c][2,7]naphthyridinones c ][2,7]naphthyridinones with expected biological activity
Al-Waleedy, Safiyyah A. H.
Younis, Osama
Abdel-Hafez, Shams H.
Bakhite, Etify A.
ARKIVOC, 2024,
[14] Synthesis of 1-Formyl-3-bromo-thieno[3,4-c]pyrrole-4,6-dione and the Application in A2-A1-D-A1-A2 Type Non-Fullerene Acceptor
Li, Jianfeng
Li, Feng
Zhang, Bao
Zhou, Erjun
JOURNAL OF PHYSICAL CHEMISTRY C, 2020, 124 (18): : 9795 - 9801
[15] Tosylmethylisocyanide (TosMIC) [3+2] cycloaddition reactions: A facile Van Leusen protocol for the synthesis of the new class of spirooxazolines, spiropyrrolines and Chromeno[3,4-c]pyrrols
Shaabani, Ahmad
Sepahvand, Heshmatollah
Bazgir, Ayoob
Khavasi, Hamid Reza
TETRAHEDRON, 2018, 74 (49) : 7058 - 7067
[16] Synthesis of new pyrido[4′,3′:4,5]thieno[2,3-d]-1,2,4-triazolo[3,4-c]pyrimidines and a 5,6-dihydro-1,2,4-triazolo[4",3":1′,2′]pyrido[4′,3′:4,5]thieno[2,3-d]-pyrimidine ring system
Ahmed, EK
Gohar, AMN
Ameen, MA
PHARMAZIE, 2000, 55 (01): : 31 - 34
[17] Synthesis of pyrano[3,4-c]thieno[3,2-e][1,2,4]triazolo[4,3-a]pyridines, representatives of a new fused heterocyclic system
Paronikyan, Ervand G.
Dashyan, Shushanik Sh.
Mamyan, Suren S.
MENDELEEV COMMUNICATIONS, 2020, 30 (02) : 183 - 184
[18] A FACILE AND UNEXPECTED SYNTHESIS OF 2 NOVEL CONDENSED HETEROCYCLES - 1,1,4,4-TETRAMETHYL-1H,4H-THIENO[3,4-C)THIOPHENE AND 1,1,4,4-TETRAMETHYL-1H,4H-SELENOLO[3,4-C]SELENOPHENE
BRAVERMAN, S
FREUND, M
GOLDBERG, I
TETRAHEDRON LETTERS, 1980, 21 (37) : 3617 - 3620
[19] Synthesis and neurotropic activity of 6-thio-substituted pyrano[3,4-c]pyridine and 1-aminopyrano[4,3-d]-thieno[2,3-b]pyridine derivatives and 9-substituted pyrido[2,3-b]thieno[3,2-d]pyrimidines
E. G. Paronikyan
Sh. F. Akopyan
A. S. Noravyan
I. A. Dzhagatspanyan
I. M. Nazaryan
A. G. Akopyan
Pharmaceutical Chemistry Journal, 2010, 44 : 183 - 185
[20] Synthesis, Cytotoxicity, Antimicrobial and Docking Simulation of Novel Pyrazolo[3,4-d]pyrimidine and pyrazolo[4,3-e][1,2,4]triazolo[3,4-c]pyrimidine Derivatives
Hassaneen, Hamdi M.
Saleh, Fatma M.
Abdallah, Tayseer A.
Mohamed, Magda F.
Mohamed, Yasmin Sh
Awad, Enas M.
Abdelhamid, Ismail A.
MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2019, 19 (08) : 657 - 670

← 1 2 3 4 5 →