Design and Synthesis of Some New Quinoxaline-Based Heterocycles
被引:21
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作者:
El Azab, Islam H.
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Taif Univ, Fac Sci, Chem Dept, POB 888, At Taif 21974, Saudi Arabia
Aswan Univ, Fac Sci, Chem Dept, POB 81528, Aswan, EgyptTaif Univ, Fac Sci, Chem Dept, POB 888, At Taif 21974, Saudi Arabia
El Azab, Islam H.
[1
,2
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Elkanzi, Nadia A. A.
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Aswan Univ, Fac Sci, Chem Dept, POB 81528, Aswan, Egypt
Aljouf Univ, Fac Sci, Chem Dept, POB 2014, Aljouf, Saudi ArabiaTaif Univ, Fac Sci, Chem Dept, POB 888, At Taif 21974, Saudi Arabia
Elkanzi, Nadia A. A.
[2
,3
]
Gobouri, Adil A.
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Taif Univ, Fac Sci, Chem Dept, POB 888, At Taif 21974, Saudi ArabiaTaif Univ, Fac Sci, Chem Dept, POB 888, At Taif 21974, Saudi Arabia
Gobouri, Adil A.
[1
]
机构:
[1] Taif Univ, Fac Sci, Chem Dept, POB 888, At Taif 21974, Saudi Arabia
[2] Aswan Univ, Fac Sci, Chem Dept, POB 81528, Aswan, Egypt
[3] Aljouf Univ, Fac Sci, Chem Dept, POB 2014, Aljouf, Saudi Arabia
Considering quinoxaline as a privileged structure for developing probes of impressive therapeutic potentials, some new azole and azine conjugates of quinoxaline were synthesized. Thus, ethyl 3-amino-1,4-dihydroquinoxaline-2-carboxylate (2) was prepared as one-pot three-component product and incorporated in a series of manipulations including cyclocondensation reactions to afford a series of pharmacophoric motif conjugates 8-12, 14, 15-17, 20-23, 24-29, 30-37, and 38-43 in fair yields. The newly synthesized were characterized by IR, H-1 NMR, C-13 NMR, and mass spectral data.
机构:
King Saud Univ, Coll Pharm, Dept Pharmaceut Chem, POB 2457, Riyadh 11541, Saudi ArabiaKing Saud Univ, Coll Pharm, Dept Pharmaceut Chem, POB 2457, Riyadh 11541, Saudi Arabia
Alsaif, Nawaf A.
Obaidullah, Ahmad J.
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King Saud Univ, Coll Pharm, Dept Pharmaceut Chem, POB 2457, Riyadh 11541, Saudi ArabiaKing Saud Univ, Coll Pharm, Dept Pharmaceut Chem, POB 2457, Riyadh 11541, Saudi Arabia
Obaidullah, Ahmad J.
Alkahtani, Hamad M.
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King Saud Univ, Coll Pharm, Dept Pharmaceut Chem, POB 2457, Riyadh 11541, Saudi ArabiaKing Saud Univ, Coll Pharm, Dept Pharmaceut Chem, POB 2457, Riyadh 11541, Saudi Arabia
Alkahtani, Hamad M.
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Alanazi, Manal M.
Alharbi, Madhawi A.
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King Saud Univ, Coll Pharm, Dept Pharmaceut Chem, POB 2457, Riyadh 11541, Saudi ArabiaKing Saud Univ, Coll Pharm, Dept Pharmaceut Chem, POB 2457, Riyadh 11541, Saudi Arabia
Alharbi, Madhawi A.
Eissa, Ibrahim H.
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Al Azhar Univ, Fac Pharm Boys, Pharmaceut Med Chem & Drug Design Dept, Cairo 11884, EgyptKing Saud Univ, Coll Pharm, Dept Pharmaceut Chem, POB 2457, Riyadh 11541, Saudi Arabia
Eissa, Ibrahim H.
Dahab, Mohammed A.
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Al Azhar Univ, Fac Pharm Boys, Pharmaceut Med Chem & Drug Design Dept, Cairo 11884, EgyptKing Saud Univ, Coll Pharm, Dept Pharmaceut Chem, POB 2457, Riyadh 11541, Saudi Arabia
机构:
Univ Putra Malaysia, Fac Sci, Dept Chem, Serdang 43400, Selangor, Malaysia
Univ Putra Malaysia, Fac Sci, Integrated Chem Biophys Res, Serdang 43400, Selangor, MalaysiaUniv Putra Malaysia, Fac Sci, Dept Chem, Serdang 43400, Selangor, Malaysia
Abdulmalek, Emilia
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Faudzi, Siti Munirah Mohd
Khan, Tabrej
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Prince Sultan Univ, Coll Engn, Dept Engn Management, Riyadh 11586, Saudi ArabiaUniv Putra Malaysia, Fac Sci, Dept Chem, Serdang 43400, Selangor, Malaysia
Khan, Tabrej
Ahmed, Omar Shabbir
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Prince Sultan Univ, Coll Engn, Dept Engn Management, Riyadh 11586, Saudi ArabiaUniv Putra Malaysia, Fac Sci, Dept Chem, Serdang 43400, Selangor, Malaysia
机构:
Arizona State Univ, Magnet Resonance Res Ctr, Tempe, AZ 85287 USA
Arizona State Univ, Sch Mol Sci, Tempe, AZ 85287 USAUniv Wyoming, Dept Chem, Laramie, WY 82071 USA
Yarger, Jeffery L.
Parkinson, Bruce A.
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Univ Wyoming, Dept Chem, Laramie, WY 82071 USA
Univ Wyoming, Sch Energy Resources, Laramie, WY 82071 USAUniv Wyoming, Dept Chem, Laramie, WY 82071 USA