SYNTHESIS OF 4-HYDROXY-3-SUBSTITUTED COUMARINS OF EXPECTED BIOLOGICAL ACTIVITY AND THEIR REACTIONS WITH SOME NUCLEOPHILES
ABD EL-GHAFFAR, N., DAWOOD, N., ABD EL-SALAM, F., FARRAG, A. (2008). SYNTHESIS OF 4-HYDROXY-3-SUBSTITUTED COUMARINS OF EXPECTED BIOLOGICAL ACTIVITY AND THEIR REACTIONS WITH SOME NUCLEOPHILES. EKB Journal Management System, 19(Issue A-2), 213-224. doi: 10.21608/absb.2008.10837
NAHED F. ABD EL-GHAFFAR; NADIA T. DAWOOD; FATMA H. ABD EL-SALAM; AWTIF E. FARRAG. "SYNTHESIS OF 4-HYDROXY-3-SUBSTITUTED COUMARINS OF EXPECTED BIOLOGICAL ACTIVITY AND THEIR REACTIONS WITH SOME NUCLEOPHILES". EKB Journal Management System, 19, Issue A-2, 2008, 213-224. doi: 10.21608/absb.2008.10837
ABD EL-GHAFFAR, N., DAWOOD, N., ABD EL-SALAM, F., FARRAG, A. (2008). 'SYNTHESIS OF 4-HYDROXY-3-SUBSTITUTED COUMARINS OF EXPECTED BIOLOGICAL ACTIVITY AND THEIR REACTIONS WITH SOME NUCLEOPHILES', EKB Journal Management System, 19(Issue A-2), pp. 213-224. doi: 10.21608/absb.2008.10837
ABD EL-GHAFFAR, N., DAWOOD, N., ABD EL-SALAM, F., FARRAG, A. SYNTHESIS OF 4-HYDROXY-3-SUBSTITUTED COUMARINS OF EXPECTED BIOLOGICAL ACTIVITY AND THEIR REACTIONS WITH SOME NUCLEOPHILES. EKB Journal Management System, 2008; 19(Issue A-2): 213-224. doi: 10.21608/absb.2008.10837

SYNTHESIS OF 4-HYDROXY-3-SUBSTITUTED COUMARINS OF EXPECTED BIOLOGICAL ACTIVITY AND THEIR REACTIONS WITH SOME NUCLEOPHILES

Al-Azhar Bulletin of Science
Article 16, Volume 19, Issue A-2, December 2008, Page 213-224  XML PDF (297.06 K)
Document Type: Original Article
DOI: 10.21608/absb.2008.10837
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Authors
NAHED F. ABD EL-GHAFFAR* ; NADIA T. DAWOOD; FATMA H. ABD EL-SALAM; AWTIF E. FARRAG
Chemistry Department, Faculty of Science, Al-Azhar University, Nasr City, Cairo
Abstract
3-Acetyl-4-hydroxy substituted coumarins (IIa-c) were prepared. Their reactions with hydrazines in DMF gave the corresponding 4-hydroxy -(3-substituted pyrazolin-3-yl)coumarins (IVa-f)  via the intermediate hydrazone (III). Their reaction with hydroxylamine hydrochloride gave the corresponding isoxazol-3-yl coumarin (VIa-c) and (VIIa,b) via the oxime intermediate (V). Reaction of II with aromatic aldehydes gave the corresponding chalcone derivatives (VIIIa-k) which were reacted with hydrazines and hydroxyl amine hydrochloride and gave (IXa)  and (Xa-c). Condensation of (IIa-c)with aromatic aldehydes, malononitrilein the presence ammonium acetate yielded the corresponding 3-cyano-4-aryl nictoinamido-6-yl-coumarin (XIa-f).
4-Hydroxy comumarin (1a-c) on treatment with POCl3 in DMF give the corresponding 4-Chloro-3-formyl coumarin (XIIa-c) which on treatment with sod azide gave the corresponding 4-azido-3-formyl coumarin (XIIIa-c). 4-chloro-3-formyl coumarine (XII )on treatment with hydrazine gave pyrazolo coumarin derivatives (XIVa-d) and on treatment with hydroxylamine hydrochloride gave 4-chloro-3-aldo oxime  coumarin derivatives (XVa,b).On treatment of 4-azido-3-formyl coumarin with active methylene compounds such as malononitrile and ethyl cyanocetate derivatives gave (XVIa-d) respectively.
The antibacterial and antifungal activities of some compounds have been described.
Keywords
4-HYDROXY-3-SUBSTITUTED
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