Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

Synthesis and Antibacterial Evaluation of Some Novel Phenylthiazolyl-Quinqzolin-4(3h)-One Derivative


Affiliations
1 Ultra College of Pharmacy, Madurai, Tamil Nadu, India
     

   Subscribe/Renew Journal


The present work deals with synthesis and evaluation of some novel phenylthiazole and quinazoline combination derivatives of biological interest. The reaction of acetophenone with thiourea formed 4-phenylthiazol-2-amine (I) was refluxed with N-chloroacetyl anthranillic acid (II) in the presence of K2CO3 in dry ethanol under anhydrous condition yields 2-chloromethyl-3-[4-(phenyl)thiazol-2-yl]-quinazolin-4(3H)one(III). The 2-chloromethyl-3-[4-(phenyl) thiazol-2-yl] quinazolin-4(3H)–one(III) and respective aromatic amines was refluxed in dry pyridine and acetic anhydride formed N-3-[4-(4–phenyl) thiazol–2–yl]-[2-(substituted amino) methyl] quinazoline-4 (3H)-one derivatives (IV).The synthesized compounds are to be screened for antibacterial activity.
Subscription Login to verify subscription
User
Notifications
Font Size


Abstract Views: 215

PDF Views: 0




  • Synthesis and Antibacterial Evaluation of Some Novel Phenylthiazolyl-Quinqzolin-4(3h)-One Derivative

Abstract Views: 215  |  PDF Views: 0

Authors

Hemant Badwaik
Ultra College of Pharmacy, Madurai, Tamil Nadu, India
Sandeep Sonkar
Ultra College of Pharmacy, Madurai, Tamil Nadu, India
Mukesh Singh
Ultra College of Pharmacy, Madurai, Tamil Nadu, India
Suresh Rajpal
Ultra College of Pharmacy, Madurai, Tamil Nadu, India
Dharamveer Sisodiya
Ultra College of Pharmacy, Madurai, Tamil Nadu, India
Ajit Pandey
Ultra College of Pharmacy, Madurai, Tamil Nadu, India

Abstract


The present work deals with synthesis and evaluation of some novel phenylthiazole and quinazoline combination derivatives of biological interest. The reaction of acetophenone with thiourea formed 4-phenylthiazol-2-amine (I) was refluxed with N-chloroacetyl anthranillic acid (II) in the presence of K2CO3 in dry ethanol under anhydrous condition yields 2-chloromethyl-3-[4-(phenyl)thiazol-2-yl]-quinazolin-4(3H)one(III). The 2-chloromethyl-3-[4-(phenyl) thiazol-2-yl] quinazolin-4(3H)–one(III) and respective aromatic amines was refluxed in dry pyridine and acetic anhydride formed N-3-[4-(4–phenyl) thiazol–2–yl]-[2-(substituted amino) methyl] quinazoline-4 (3H)-one derivatives (IV).The synthesized compounds are to be screened for antibacterial activity.