Synthesis of pyrimidine linked heterocyclic scaffolds by intramolecular cyclization and study of biological potential (Record no. 19253)

000 -LEADER
fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20230428113705.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 230428b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 15679
Author Deohate, Pradip P.
245 ## - TITLE STATEMENT
Title Synthesis of pyrimidine linked heterocyclic scaffolds by intramolecular cyclization and study of biological potential
250 ## - EDITION STATEMENT
Volume, Issue number Vol.61(5), May
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. New Delhi
Name of publisher, distributor, etc. CSIR
Year 2022
300 ## - PHYSICAL DESCRIPTION
Pagination 551-557p.
520 ## - SUMMARY, ETC.
Summary, etc. Synthesis of some interesting pyrimidine linked heterocyclic scaffolds by intramolecular cyclization has been worked out. Initially compound (4,6-dimethyl-pyrimidin-2-yl-amino)-acetic acid hydrazide has been prepared by reacting 2-amino-4,6-dimethyl pyrimidine with ethyl chloroacetate, followed by condensation with hydrazine hydrate. It has then been treated with N-aryl/alkyl isothiocyanates, followed by intramolecular cyclization using alkaline ethanolic solution of I2 with KI, o-phosphoric acid and aqueous KOH to afford respective heterocyclic compounds with differently substituted pharmacophores viz. (5-aryl/alkyl-amino-[1,3,4]-oxadiazol-2-yl-methyl)-(4,6-dimethyl-pyrimidin-2-yl)-amines, (5-aryl/alkyl-amino-[1,3,4]-thiadiazol-2-yl-methyl)-(4,6-dimethyl-pyrimidin-2-yl)-amines and (4-aryl/alkyl-5-mercapto-[1,2,4]-triazol-3-yl-methyl)-(4,6-dimethyl-pyrimidin-2-yl)-amines. Developments during the synthesis have been monitored by TLC. Constitution of synthesized compounds have been delineated in accordance with equivalent weight, elemental assay,chemical transformation and IR, 1H NMR and mass spectral investigations. Title compounds have been tested for their biological potential.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 5009
Topical term or geographic name entry element GENERAL CHEMISTRY
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 15677
Co-Author Palaspagar, Kalpana A.
773 0# - HOST ITEM ENTRY
Title Indian journal of chemistry (Section B)
International Standard Serial Number 0019-5103
Place, publisher, and date of publication New Delhi NISCAIR-CSIR 2005
856 ## - ELECTRONIC LOCATION AND ACCESS
URL http://op.niscpr.res.in/index.php/IJC/article/view/63648
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Koha item type Articles Abstract Database
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Permanent Location Current Location Shelving location Date acquired Barcode Date last seen Price effective from Koha item type
          School of Pharmacy School of Pharmacy Archieval Section 2023-04-28 2023-0744 2023-04-28 2023-04-28 Articles Abstract Database
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