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One-pot synthesis of 2,6-diaryl-4,5-dihydropyridazin-3(2H)-ones: Copper catalyzed annulation of aldehydes, arylhydrazines and 3-acryloyloxazolidin-2-one
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作者:

Zhao, Jianbo
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机构: East China Univ Sci & Technol, State Key Lab Bioengn Reactor, Shanghai Key Lab New Drug Design, 130 Mei long Rd, Shanghai 200237, Peoples R China

Lei, Shengshu
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机构: East China Univ Sci & Technol, State Key Lab Bioengn Reactor, Shanghai Key Lab New Drug Design, 130 Mei long Rd, Shanghai 200237, Peoples R China

Wu, Min
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机构: East China Univ Sci & Technol, State Key Lab Bioengn Reactor, Shanghai Key Lab New Drug Design, 130 Mei long Rd, Shanghai 200237, Peoples R China

Pang, Can
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机构: East China Univ Sci & Technol, State Key Lab Bioengn Reactor, Shanghai Key Lab New Drug Design, 130 Mei long Rd, Shanghai 200237, Peoples R China

Li, Hao
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East China Univ Sci & Technol, State Key Lab Bioengn Reactor, Shanghai Key Lab New Drug Design, 130 Mei long Rd, Shanghai 200237, Peoples R China East China Univ Sci & Technol, State Key Lab Bioengn Reactor, Shanghai Key Lab New Drug Design, 130 Mei long Rd, Shanghai 200237, Peoples R China
机构:
[1] East China Univ Sci & Technol, State Key Lab Bioengn Reactor, Shanghai Key Lab New Drug Design, 130 Mei long Rd, Shanghai 200237, Peoples R China
关键词:
Annulation;
Copper;
One;
-pot;
Pyridazinones;
PROGESTERONE-RECEPTOR LIGANDS;
BIOLOGICAL EVALUATION;
PHTHALAZINONE DERIVATIVES;
CARDIOTONIC AGENTS;
PYRIDAZINONE;
4,5-DIHYDRO-3(2H)-PYRIDAZINONES;
SELECTIVITY;
AFFINITY;
SERIES;
D O I:
10.1016/j.tetlet.2023.154473
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
The three-component synthesis of pyridazinones from aldehydes, arylhydrazines and 3-acryloyloxazo-lidin-2-one catalyzed by Cu(OTf)2 has been developed. This strategy exhibits high tolerance towards many functional groups including various aliphatic, aromatic and hetero-aromatic aldehydes to give 2,6-diaryl-4,5-dihydropyridazin-3(2H)-one products in moderate to high yields.(c) 2023 Elsevier Ltd. All rights reserved.
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[1]
Synthesis and biological evaluation of some novel 6-aryl-2-(p-sulfamylphenyl)-4,5-dihydropyridazin-3(2H)-ones as anti-cancer, antimicrobial, and anti-inflammatory agents
[J].
Ahmad, Shamim
;
Rathish, I. G.
;
Bano, Sameena
;
Alam, M. S.
;
Javed, Kalim
.
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY,
2010, 25 (02)
:266-271

Ahmad, Shamim
论文数: 0 引用数: 0
h-index: 0
机构:
Jamia Hamdard, Fac Sci, Dept Chem, New Delhi 110062, India Jamia Hamdard, Fac Sci, Dept Chem, New Delhi 110062, India

Rathish, I. G.
论文数: 0 引用数: 0
h-index: 0
机构:
Jamia Hamdard, Fac Sci, Dept Chem, New Delhi 110062, India Jamia Hamdard, Fac Sci, Dept Chem, New Delhi 110062, India

Bano, Sameena
论文数: 0 引用数: 0
h-index: 0
机构:
Jamia Hamdard, Fac Sci, Dept Chem, New Delhi 110062, India Jamia Hamdard, Fac Sci, Dept Chem, New Delhi 110062, India

Alam, M. S.
论文数: 0 引用数: 0
h-index: 0
机构:
Jamia Hamdard, Fac Sci, Dept Chem, New Delhi 110062, India Jamia Hamdard, Fac Sci, Dept Chem, New Delhi 110062, India

Javed, Kalim
论文数: 0 引用数: 0
h-index: 0
机构:
Jamia Hamdard, Fac Sci, Dept Chem, New Delhi 110062, India Jamia Hamdard, Fac Sci, Dept Chem, New Delhi 110062, India
[2]
Discovery of 6-oxo-3-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)-1(6H)pyridazinebutanoic acid (FK838):: A novel non-xanthine adenosine A1 receptor antagonist with potent diuretic activity
[J].
Akahane, A
;
Katayama, H
;
Mitsunaga, T
;
Kato, T
;
Kinoshita, T
;
Kita, Y
;
Kusunoki, T
;
Terai, T
;
Yoshida, K
;
Shiokawa, Y
.
JOURNAL OF MEDICINAL CHEMISTRY,
1999, 42 (05)
:779-783

Akahane, A
论文数: 0 引用数: 0
h-index: 0
机构:
Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan

Katayama, H
论文数: 0 引用数: 0
h-index: 0
机构:
Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan

Mitsunaga, T
论文数: 0 引用数: 0
h-index: 0
机构:
Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan

Kato, T
论文数: 0 引用数: 0
h-index: 0
机构:
Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan

Kinoshita, T
论文数: 0 引用数: 0
h-index: 0
机构:
Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan

Kita, Y
论文数: 0 引用数: 0
h-index: 0
机构:
Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan

Kusunoki, T
论文数: 0 引用数: 0
h-index: 0
机构:
Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan

Terai, T
论文数: 0 引用数: 0
h-index: 0
机构:
Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan

Yoshida, K
论文数: 0 引用数: 0
h-index: 0
机构:
Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan

Shiokawa, Y
论文数: 0 引用数: 0
h-index: 0
机构:
Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan Fujisawa Pharmaceut Co Ltd, Med Chem Res Labs, Yodogawa Ku, Osaka 5328514, Japan
[3]
First synthesis of 4,5-dihydro-3(2H)-pyridazinones via Zn-mediated hydrohydrazination
[J].
Alex, Karolin
;
Tillack, Annegret
;
Schwarz, Nicolle
;
Beller, Matthias
.
TETRAHEDRON LETTERS,
2008, 49 (31)
:4607-4609

Alex, Karolin
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany

Tillack, Annegret
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany

Schwarz, Nicolle
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany

Beller, Matthias
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany
[4]
Pyridazin-3(2H)-ones: the versatile pharmacophore of medicinal significance
[J].
Bansal, Ranju
;
Thota, Sridhar
.
MEDICINAL CHEMISTRY RESEARCH,
2013, 22 (06)
:2539-2552

Bansal, Ranju
论文数: 0 引用数: 0
h-index: 0
机构:
Panjab Univ, Univ Inst Pharmaceut Sci, Chandigarh 160014, India Panjab Univ, Univ Inst Pharmaceut Sci, Chandigarh 160014, India

Thota, Sridhar
论文数: 0 引用数: 0
h-index: 0
机构:
Panjab Univ, Univ Inst Pharmaceut Sci, Chandigarh 160014, India Panjab Univ, Univ Inst Pharmaceut Sci, Chandigarh 160014, India
[5]
Synthesis and biological evaluation of some novel sulfamoylphenyl-pyridazinone as anti-inflammatory agents (Part-II)
[J].
Bashir, Rafia
;
Yaseen, Shafiya
;
Ovais, Syed
;
Ahmad, Shamim
;
Hamid, Hinna
;
Alam, M. S.
;
Samim, Mohammad
;
Javed, Kalim
.
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY,
2012, 27 (01)
:92-96

Bashir, Rafia
论文数: 0 引用数: 0
h-index: 0
机构:
Jamia Hamdard, Dept Chem, Fac Sci, New Delhi 110062, India Jamia Hamdard, Dept Chem, Fac Sci, New Delhi 110062, India

Yaseen, Shafiya
论文数: 0 引用数: 0
h-index: 0
机构:
Jamia Hamdard, Dept Chem, Fac Sci, New Delhi 110062, India Jamia Hamdard, Dept Chem, Fac Sci, New Delhi 110062, India

Ovais, Syed
论文数: 0 引用数: 0
h-index: 0
机构:
Jamia Hamdard, Dept Chem, Fac Sci, New Delhi 110062, India Jamia Hamdard, Dept Chem, Fac Sci, New Delhi 110062, India

Ahmad, Shamim
论文数: 0 引用数: 0
h-index: 0
机构:
Jamia Hamdard, Dept Chem, Fac Sci, New Delhi 110062, India Jamia Hamdard, Dept Chem, Fac Sci, New Delhi 110062, India

Hamid, Hinna
论文数: 0 引用数: 0
h-index: 0
机构:
Jamia Hamdard, Dept Chem, Fac Sci, New Delhi 110062, India Jamia Hamdard, Dept Chem, Fac Sci, New Delhi 110062, India

Alam, M. S.
论文数: 0 引用数: 0
h-index: 0
机构:
Jamia Hamdard, Dept Chem, Fac Sci, New Delhi 110062, India Jamia Hamdard, Dept Chem, Fac Sci, New Delhi 110062, India

Samim, Mohammad
论文数: 0 引用数: 0
h-index: 0
机构:
Jamia Hamdard, Dept Chem, Fac Sci, New Delhi 110062, India Jamia Hamdard, Dept Chem, Fac Sci, New Delhi 110062, India

Javed, Kalim
论文数: 0 引用数: 0
h-index: 0
机构:
Jamia Hamdard, Dept Chem, Fac Sci, New Delhi 110062, India Jamia Hamdard, Dept Chem, Fac Sci, New Delhi 110062, India
[6]
α1-adrenoceptor antagonists.: 5.: Pyridazinone-arylpiperazines.: Probing the influence on affinity and selectivity of both ortho-alkoxy groups at the arylpiperazine moiety and cyclic substituents at the pyridazinone nucleus
[J].
Betti, L
;
Floridi, M
;
Giannaccini, G
;
Manetti, F
;
Strappaghetti, G
;
Tafi, A
;
Botta, M
.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS,
2003, 13 (02)
:171-173

Betti, L
论文数: 0 引用数: 0
h-index: 0
机构: Univ Perugia, Ist Chim & Tecnol Farm, I-06123 Perugia, Italy

Floridi, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Perugia, Ist Chim & Tecnol Farm, I-06123 Perugia, Italy

论文数: 引用数:
h-index:
机构:

论文数: 引用数:
h-index:
机构:

Strappaghetti, G
论文数: 0 引用数: 0
h-index: 0
机构: Univ Perugia, Ist Chim & Tecnol Farm, I-06123 Perugia, Italy

Tafi, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Perugia, Ist Chim & Tecnol Farm, I-06123 Perugia, Italy

Botta, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Perugia, Ist Chim & Tecnol Farm, I-06123 Perugia, Italy
[7]
CARDIOTONIC AGENTS .1. 4,5-DIHYDRO-6-[4-(1H-IMIDAZOL-1-YL)PHENYL]-3(2H)-PYRIDAZINONES - NOVEL POSITIVE INOTROPIC AGENTS FOR THE TREATMENT OF CONGESTIVE HEART-FAILURE
[J].
BRISTOL, JA
;
SIRCAR, I
;
MOOS, WH
;
EVANS, DB
;
WEISHAAR, RE
.
JOURNAL OF MEDICINAL CHEMISTRY,
1984, 27 (09)
:1099-1101

BRISTOL, JA
论文数: 0 引用数: 0
h-index: 0
机构:
WARNER LAMBERT PARKE DAVIS,PHARMACEUT RES,DEPT PHARMACOL,ANN ARBOR,MI 48105 WARNER LAMBERT PARKE DAVIS,PHARMACEUT RES,DEPT PHARMACOL,ANN ARBOR,MI 48105

SIRCAR, I
论文数: 0 引用数: 0
h-index: 0
机构:
WARNER LAMBERT PARKE DAVIS,PHARMACEUT RES,DEPT PHARMACOL,ANN ARBOR,MI 48105 WARNER LAMBERT PARKE DAVIS,PHARMACEUT RES,DEPT PHARMACOL,ANN ARBOR,MI 48105

MOOS, WH
论文数: 0 引用数: 0
h-index: 0
机构:
WARNER LAMBERT PARKE DAVIS,PHARMACEUT RES,DEPT PHARMACOL,ANN ARBOR,MI 48105 WARNER LAMBERT PARKE DAVIS,PHARMACEUT RES,DEPT PHARMACOL,ANN ARBOR,MI 48105

EVANS, DB
论文数: 0 引用数: 0
h-index: 0
机构:
WARNER LAMBERT PARKE DAVIS,PHARMACEUT RES,DEPT PHARMACOL,ANN ARBOR,MI 48105 WARNER LAMBERT PARKE DAVIS,PHARMACEUT RES,DEPT PHARMACOL,ANN ARBOR,MI 48105

WEISHAAR, RE
论文数: 0 引用数: 0
h-index: 0
机构:
WARNER LAMBERT PARKE DAVIS,PHARMACEUT RES,DEPT PHARMACOL,ANN ARBOR,MI 48105 WARNER LAMBERT PARKE DAVIS,PHARMACEUT RES,DEPT PHARMACOL,ANN ARBOR,MI 48105
[8]
Pyridazine derivatives.: Part 33:: Sonogashira approaches in the synthesis of 5-substituted-6-phenyl-3(2H)-pyridazinones
[J].
Coelho, A
;
Sotelo, E
;
Raviña, E
.
TETRAHEDRON,
2003, 59 (14)
:2477-2484

论文数: 引用数:
h-index:
机构:

Sotelo, E
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Santiago de Compostela, Fac Farm, Dept Quim Organ, Lab Quim Farmaceut, Santiago De Compostela 15782, Spain Univ Santiago de Compostela, Fac Farm, Dept Quim Organ, Lab Quim Farmaceut, Santiago De Compostela 15782, Spain

Raviña, E
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Santiago de Compostela, Fac Farm, Dept Quim Organ, Lab Quim Farmaceut, Santiago De Compostela 15782, Spain Univ Santiago de Compostela, Fac Farm, Dept Quim Organ, Lab Quim Farmaceut, Santiago De Compostela 15782, Spain
[9]
NONSTEROIDAL PROGESTERONE-RECEPTOR LIGANDS .2. HIGH-AFFINITY LIGANDS WITH SELECTIVITY FOR BONE CELL PROGESTERONE RECEPTORS
[J].
COMBS, DW
;
REESE, K
;
CORNELIUS, LAM
;
GUNNET, JW
;
CRYAN, EV
;
GRANGER, KS
;
JORDAN, JJ
;
DEMAREST, KT
.
JOURNAL OF MEDICINAL CHEMISTRY,
1995, 38 (25)
:4880-4884

COMBS, DW
论文数: 0 引用数: 0
h-index: 0
机构: The R. W. Johnson Pharmaceutical Research Institute, Raritan, New Jersey 08869-0602

REESE, K
论文数: 0 引用数: 0
h-index: 0
机构: The R. W. Johnson Pharmaceutical Research Institute, Raritan, New Jersey 08869-0602

CORNELIUS, LAM
论文数: 0 引用数: 0
h-index: 0
机构: The R. W. Johnson Pharmaceutical Research Institute, Raritan, New Jersey 08869-0602

GUNNET, JW
论文数: 0 引用数: 0
h-index: 0
机构: The R. W. Johnson Pharmaceutical Research Institute, Raritan, New Jersey 08869-0602

CRYAN, EV
论文数: 0 引用数: 0
h-index: 0
机构: The R. W. Johnson Pharmaceutical Research Institute, Raritan, New Jersey 08869-0602

GRANGER, KS
论文数: 0 引用数: 0
h-index: 0
机构: The R. W. Johnson Pharmaceutical Research Institute, Raritan, New Jersey 08869-0602

JORDAN, JJ
论文数: 0 引用数: 0
h-index: 0
机构: The R. W. Johnson Pharmaceutical Research Institute, Raritan, New Jersey 08869-0602

DEMAREST, KT
论文数: 0 引用数: 0
h-index: 0
机构: The R. W. Johnson Pharmaceutical Research Institute, Raritan, New Jersey 08869-0602
[10]
NONSTEROIDAL PROGESTERONE-RECEPTOR LIGANDS .1. 3-ARYL-1-BENZOYL-1,4,5,6-TETRAHYDROPYRIDAZINES
[J].
COMBS, DW
;
REESE, K
;
PHILLIPS, A
.
JOURNAL OF MEDICINAL CHEMISTRY,
1995, 38 (25)
:4878-4879

COMBS, DW
论文数: 0 引用数: 0
h-index: 0
机构: The R. W. Johnson Pharmaceutical Research Institute, Raritan, New Jersey 08869-0602

REESE, K
论文数: 0 引用数: 0
h-index: 0
机构: The R. W. Johnson Pharmaceutical Research Institute, Raritan, New Jersey 08869-0602

PHILLIPS, A
论文数: 0 引用数: 0
h-index: 0
机构: The R. W. Johnson Pharmaceutical Research Institute, Raritan, New Jersey 08869-0602