STUDIES OF OXAZOLE , BENZIMIDAZOLE, OXADIAZOLE AND
                               RELATED COMPOUNDS
THESIS SUBMITTED TO THE UNIVERSITY OF MUMBAI
       FOR THE DEGREE OF DOCTOR OF PHILOSOPHY
         FACULTY OF SCIENCE (ORGANIC CHEMISTRY)
                                PATKAR COLLEGE

                                              2008
 SYNOPSIS
 OF THE THESIS TO BE SUBMITTED TO
 THE UNIVERSITY OF MUMBAI

 FOR THE DEGREE OF DOCTOR OF PHYLOSOPHY IN THE FACULTY
 OF SCIENCE (ORGANIC CHEMISTRY)

 NAME OF THE STUDENT    : VIBHA JAGDEVPRASAD PANDEY
 TITLE OF THESIS :“STUDIES IN
 OXAZOLE, IMIDAZOLE, BENZIMIDAZOLE AND RELATED
 COMPOUNDS”.

 NAME AND DESIGNATION : Dr.UDAY C. MASHELKAR M.Sc. Ph.D.
 THE OF GUIDING TEACHER PRINCIPAL, PATKAR
 COLLEGE,    GOREGAON (W)

 PLACE OF RESEARCH    : ORGANIC RESAERCH LABORTORY.
 PATKAR COLLEGE, GOREGOAN (W).

 NUMBER AND DATE OF      : 17 / 6th DECEMBER 2005
 REGISTRATION
 DATE OF SUBMISSION OF   : 20th DECEMBER 2007
 Compounds based on coumarin and chromone ring system
    are one of the most extensively investigated and
    commercially significant groups of organic compounds. In
    recent years coumarin containing crown ethers and
    macrocyclic systems has been exploited in the area of metal
    ion sensors1 and number of these product shows marked
    physiological impact2. In addition coumarins are also of
    considerable biological and medicinal interest. It is found
    that coumarin plays important role in enzymatic oxidation3
    and shows antioxidative, perioxidative effect4.

 Nitrogen containing heterocycles being another important group of
  heterocycles5, these compounds are widely distributed in nature. These
  compounds playing a vital role in the metabolic activity of all living
  cells e.g. the pyrimidine and purine bases of the genetic materials; the
  essential amino acids; the vitamins and coenzymes. Imidazole and
  benzimidazole are the important group of compounds6.
  Benzimidazoles are known to have varied biological activity and among
  them 2- substituted benzimidazolees are found to be more potent.7

 Owing to the importance of these systems in
  pharmacological, commercial, analytical and industrial applications;
  it’s significant to design and synthesize novel heterocycles of these
  classes. Keeping this in mind, we targeted to synthesize coumarin with
  benzimidazole, benzisooxazole, oxazole and oxodiazole as substitution
  at four position of coumarin. At the same time these substitutions were
  attached with chromone ring. As wide application of chromone and
  coumarin were seen in the host-guest chemistry and metal ions
  sensors8. We synthesized some of the coumarin and chromone based
  podands and their complexes with transition metal ions. Podands are
  linear multidentate legands. These podands are similar to salen and
  smdpt9.

 The synthetic strategy employed for the purpose is summarized below.
 Chromone aldehyde and coumarin aldehydes were prepared as per the
  literature10, from phenols by Pechmann condensation and Vilsmeier-Hack
  reaction11.

 These aldehydes were condensed with hydrazides of isooxazole 2-acetic acid
  esters, and subsequent cyclization in acidic medium gives the desired
  oxadiazole derivatives.

 Another synthetic route employed the alkylation of imidazole with
  chloroethylacetate their hydrazide formation.

 Furthermore the podands were prepared from Ethylenediamine and o-
  phynelenediamine (OPDA) to yield salen and smdpt type of compound.
  Complexes of these ligands with transition metal ions were studied.

 This work is presented through five chapters.
 Chapter one is introductory in nature dealing with
    coumarins, imidazoles, isooxazoles and oxadiazoles, their general
    method of synthesis, characterization and reactions that lead to
    modified and highly functionalized compounds, their applications in
    various fields of interest.

         Chapter two and three deals with theoretical and experimental
    part of synthesis leading to coumarin and chromone derivatives with
    imidazole, oxazole, oxadiazole.

        Chapter four is about the tweezers and ligands synthesis of
    benzimidazole, oxazole and chromene.

 Chapter five is regarding the application part of synthesized molecule
    i.e. complexation studies of the ligands with transition metals and their
    biological activity.
O

        OH                                     OH
R
                               R
                                       O       O
                                                   (1)



                                                   N
                       O                               N
                                                       H

    R                              R
                   O       O                   O       O   (3)
             (2)
                           Scheme-1
N                            N                                   N

              N                            N                                   N       H
              H                                    O                                   N NH
                                                                                           2

R                 R                            O       R                           O
      O       O                    O       O                           O       O
    (3)


          N
                                                               N
              N
                      N                                            N       H
                          N                                                N N
R                 O
     O        O                                R                       O
                                                           O       O
                                                                                          R,
          (4)
                              R,
                          Scheme-2
O

                                       O                    O         R
                               O               R    O
R
          O       O
    (3)
              +                N                    N
    O
                      OH           O       O            N       O
          N
          H
                  O
                                                                (5)
                                                   R,
                           Scheme-3
O

           OH

     N
 O
           N                   N           N
                     O             O
               N               N            N
               H               H            H
       N                   N           N
   O                   O           O
(6)                 (7)                    (8)

                   Scheme-4
N                                                                          N
                                                N

              N                                                                      N
                                                N
              H
                                                                                 N                O
    N                                       N           O
O                                                                            O
                                        O                                                HN
        (6)                                         O                                         NH2



              N                                                     N


              N                                                     N
                                                                                                      R
                                        R                       N                O
    N                   N
O                           N                               O
                    O                                                   HN
                                                                             N
                                                                                                  O
                                    O
                  (9)                                                                         O
                                O
                                        Scheme-5
O                          O                           O
                OH                         O                                NH2
                                                                       NH
            N                          N
        O                                                      N
                                   O                       O
                                                                   R
            N N
                            O
                                                       O                     O
            O
                        O                                  N
    N                                                  N                          O
                                                       H
O                                                  N
                    R                          O
        (10)
                                Scheme-6
OH
                               HO                   O     O       AcO            O       O


            HO



                               O
                                                                    HO               O       O
                 HO                O       O



                                                                        O

    O

        O                              O                                                     O                 O   O
                                                              O             O    O
O            O        O    O               O        O                            O

                                                                                             O
                                                              O
                                                                   (13)                                 (14)
        (11)                           (12)

                  OH                       OH       O
                                                                                 O

                                                                                                 O

        HO                     HO
                                                                            HO
                                                                                                 (15)
                                               O              O

                                                          O

                                   HO
                                                   (16)
                                           Scheme-7
O


                   O
                                                               N       O        O
NH                     O

     +                                                                                O
           O               O       O
NH                                                     N

                                                           O

         [(11), (2), (14), (16)]                   O           O       O
                                                                               (17)


                                                                           O                 O   O



                                                                           O
                                                               N
     NH                O               O    O
                                                                           O
      +    O                                                       N
     NH                                                                                              O
                       O
                  [(11), (2), (14), (16)]
                                                                                      (18)

                                       Scheme- 8
REFERENCES:
   Valeur B. Habib Jivan J.L. J. Photoch. Photobio. A 116, 127,(1998).
   Miyake. Joshi. J. Agri. Food. Chem. 48(8), 3151, (1999).
   Swain C. G., Thripathy P. C., Ind. J. Plant. Physiology. I4(3), (1999), 157.
   Liu Z. Q., Yu. W., Chem. Phy. Lipids, 103(1,2), 125 (1999).
   Grimmet. M. R, “Comprehensive Heterocyclic
    Chemistry”, Potts.K.T.(Ed), Katrizky. A.R. & Rees. K. W.(Gen.Eds.), Pergamon
    Press, Oxford, Vol.5, Chapter 4, 457, (1984).
   Preston P. N. Chem. Rev., 74, 279, (1974).
   Preston P. N (ED) “Benzimidazoles and Congeneric Tricyclic
    Compounds”, (Wiley Interscience, New York) Part2, Chapter 10, 531 (1980).
   a) Willem. Verboom David N. Reinhoudt, Chem. Soc. Perkin. Tran 2. 135 (1995).
    b) Tyagi et.al. I.J.C. vol.78, 251 (2001).
   Ind. Ac. Sci. A. 567 (1938).
   Sethna. Sm, Shah R.C. J. Chem. Soc. 228., (1938).
    Horning, E. C. in Organic synthesis, Vol. III, Wiley, New York, 281(1955).
Thanks
 vibhagreat2007@gmail.com
 Tel 9322191450

Dr vibha bhagat phd synopsis

  • 1.
    STUDIES OF OXAZOLE, BENZIMIDAZOLE, OXADIAZOLE AND RELATED COMPOUNDS THESIS SUBMITTED TO THE UNIVERSITY OF MUMBAI FOR THE DEGREE OF DOCTOR OF PHILOSOPHY FACULTY OF SCIENCE (ORGANIC CHEMISTRY) PATKAR COLLEGE 2008
  • 2.
     SYNOPSIS  OFTHE THESIS TO BE SUBMITTED TO  THE UNIVERSITY OF MUMBAI  FOR THE DEGREE OF DOCTOR OF PHYLOSOPHY IN THE FACULTY OF SCIENCE (ORGANIC CHEMISTRY)   NAME OF THE STUDENT : VIBHA JAGDEVPRASAD PANDEY  TITLE OF THESIS :“STUDIES IN OXAZOLE, IMIDAZOLE, BENZIMIDAZOLE AND RELATED COMPOUNDS”.  NAME AND DESIGNATION : Dr.UDAY C. MASHELKAR M.Sc. Ph.D.  THE OF GUIDING TEACHER PRINCIPAL, PATKAR COLLEGE, GOREGAON (W)  PLACE OF RESEARCH : ORGANIC RESAERCH LABORTORY. PATKAR COLLEGE, GOREGOAN (W).  NUMBER AND DATE OF : 17 / 6th DECEMBER 2005  REGISTRATION  DATE OF SUBMISSION OF : 20th DECEMBER 2007
  • 4.
     Compounds basedon coumarin and chromone ring system are one of the most extensively investigated and commercially significant groups of organic compounds. In recent years coumarin containing crown ethers and macrocyclic systems has been exploited in the area of metal ion sensors1 and number of these product shows marked physiological impact2. In addition coumarins are also of considerable biological and medicinal interest. It is found that coumarin plays important role in enzymatic oxidation3 and shows antioxidative, perioxidative effect4. 
  • 5.
     Nitrogen containingheterocycles being another important group of heterocycles5, these compounds are widely distributed in nature. These compounds playing a vital role in the metabolic activity of all living cells e.g. the pyrimidine and purine bases of the genetic materials; the essential amino acids; the vitamins and coenzymes. Imidazole and benzimidazole are the important group of compounds6. Benzimidazoles are known to have varied biological activity and among them 2- substituted benzimidazolees are found to be more potent.7  Owing to the importance of these systems in pharmacological, commercial, analytical and industrial applications; it’s significant to design and synthesize novel heterocycles of these classes. Keeping this in mind, we targeted to synthesize coumarin with benzimidazole, benzisooxazole, oxazole and oxodiazole as substitution at four position of coumarin. At the same time these substitutions were attached with chromone ring. As wide application of chromone and coumarin were seen in the host-guest chemistry and metal ions sensors8. We synthesized some of the coumarin and chromone based podands and their complexes with transition metal ions. Podands are linear multidentate legands. These podands are similar to salen and smdpt9.   The synthetic strategy employed for the purpose is summarized below.
  • 6.
     Chromone aldehydeand coumarin aldehydes were prepared as per the literature10, from phenols by Pechmann condensation and Vilsmeier-Hack reaction11.  These aldehydes were condensed with hydrazides of isooxazole 2-acetic acid esters, and subsequent cyclization in acidic medium gives the desired oxadiazole derivatives.  Another synthetic route employed the alkylation of imidazole with chloroethylacetate their hydrazide formation.  Furthermore the podands were prepared from Ethylenediamine and o- phynelenediamine (OPDA) to yield salen and smdpt type of compound. Complexes of these ligands with transition metal ions were studied.  This work is presented through five chapters.
  • 7.
     Chapter oneis introductory in nature dealing with coumarins, imidazoles, isooxazoles and oxadiazoles, their general method of synthesis, characterization and reactions that lead to modified and highly functionalized compounds, their applications in various fields of interest.  Chapter two and three deals with theoretical and experimental part of synthesis leading to coumarin and chromone derivatives with imidazole, oxazole, oxadiazole.  Chapter four is about the tweezers and ligands synthesis of benzimidazole, oxazole and chromene.  Chapter five is regarding the application part of synthesized molecule i.e. complexation studies of the ligands with transition metals and their biological activity.
  • 8.
    O OH OH R R O O (1) N O N H R R O O O O (3) (2) Scheme-1
  • 9.
    N N N N N N H H O N NH 2 R R O R O O O O O O O (3) N N N N N H N N N R O O O R O O O R, (4) R, Scheme-2
  • 10.
    O O O R O R O R O O (3) + N N O OH O O N O N H O (5) R, Scheme-3
  • 11.
    O OH N O N N N O O N N N H H H N N N O O O (6) (7) (8) Scheme-4
  • 12.
    N N N N N N H N O N N O O O O HN (6) O NH2 N N N N R R N O N N O N O O HN N O O (9) O O Scheme-5
  • 13.
    O O O OH O NH2 NH N N O N O O R N N O O O O O N N N O H O N R O (10) Scheme-6
  • 14.
    OH HO O O AcO O O HO O HO O O HO O O O O O O O O O O O O O O O O O O O O O (13) (14) (11) (12) OH OH O O O HO HO HO (15) O O O HO (16) Scheme-7
  • 15.
    O O N O O NH O + O O O O NH N O [(11), (2), (14), (16)] O O O (17) O O O O N NH O O O O + O N NH O O [(11), (2), (14), (16)] (18) Scheme- 8
  • 16.
    REFERENCES:  Valeur B. Habib Jivan J.L. J. Photoch. Photobio. A 116, 127,(1998).  Miyake. Joshi. J. Agri. Food. Chem. 48(8), 3151, (1999).  Swain C. G., Thripathy P. C., Ind. J. Plant. Physiology. I4(3), (1999), 157.  Liu Z. Q., Yu. W., Chem. Phy. Lipids, 103(1,2), 125 (1999).  Grimmet. M. R, “Comprehensive Heterocyclic Chemistry”, Potts.K.T.(Ed), Katrizky. A.R. & Rees. K. W.(Gen.Eds.), Pergamon Press, Oxford, Vol.5, Chapter 4, 457, (1984).  Preston P. N. Chem. Rev., 74, 279, (1974).  Preston P. N (ED) “Benzimidazoles and Congeneric Tricyclic Compounds”, (Wiley Interscience, New York) Part2, Chapter 10, 531 (1980).  a) Willem. Verboom David N. Reinhoudt, Chem. Soc. Perkin. Tran 2. 135 (1995). b) Tyagi et.al. I.J.C. vol.78, 251 (2001).  Ind. Ac. Sci. A. 567 (1938).  Sethna. Sm, Shah R.C. J. Chem. Soc. 228., (1938).  Horning, E. C. in Organic synthesis, Vol. III, Wiley, New York, 281(1955).
  • 17.