Diazotization of substituted anilines 1 with NaNO2 and Conc. HCl at 0(0) gave the diazonium chlorides 2. Coupling of substituted aryl diazonium chlorides 2 with ethyl acetoacetate in methanol gave ethyl-2-arylhydrazono-3-oxobutyrates 3. Reaction of 3 with 2-hydroxybenzo hydrazide gave the novel pyrazolone derivatives (4a-j). The newly synthesized compounds were screened for their in vitro antibacterial, antifungal and antitubercular activities. Some of the new compounds showed good antibacterial and antitubercular activity. Structures of all the new compounds were established on the basis of elemental analysis, IR, H-1 NMR and Mass spectral data.
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King Abdulaziz Univ, Jeddah Community Coll, Hlth Informat Technol Dept, POB 80283, Jeddah 21589, Saudi ArabiaKing Abdulaziz Univ, Jeddah Community Coll, Hlth Informat Technol Dept, POB 80283, Jeddah 21589, Saudi Arabia
Ahmad, Aftab
Husain, Asif
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Hamdard Univ, Dept Pharmaceut Chem, Fac Pharm, New Delhi, IndiaKing Abdulaziz Univ, Jeddah Community Coll, Hlth Informat Technol Dept, POB 80283, Jeddah 21589, Saudi Arabia
Husain, Asif
Khan, Shah Alam
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Oman Med Coll, Dept Pharm, Muscat, OmanKing Abdulaziz Univ, Jeddah Community Coll, Hlth Informat Technol Dept, POB 80283, Jeddah 21589, Saudi Arabia
Khan, Shah Alam
Mujeeb, Mohd.
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Hamdard Univ, Fac Pharm, Dept Pharmacognosy & Phytochem, New Delhi, IndiaKing Abdulaziz Univ, Jeddah Community Coll, Hlth Informat Technol Dept, POB 80283, Jeddah 21589, Saudi Arabia
Mujeeb, Mohd.
Bhandari, Anil
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Jodhpur Natl Univ, Fac Pharmaceut Sci, Dept Pharmaceut Chem, Jodhpur, Rajasthan, IndiaKing Abdulaziz Univ, Jeddah Community Coll, Hlth Informat Technol Dept, POB 80283, Jeddah 21589, Saudi Arabia