Identyfikatory
Warianty tytułu
Języki publikacji
Abstrakty
Isatins are synthetically versatile substrates, where they can be used for the synthesis of a large variety of Isatins and heterocyclic compounds. In this, the isatin were extracted from the floral material of Couroupita guianesis commonly known as an Cannon ball tree. After that, a novel heterocyclic spiro derivative having an IUPAC name N,N’-(2-oxo-3’H-spiro[indoline-3,2’-[1,3,4] thiadiazole]-3’5’-diyl)diacetamide were synthesized , which may be used as raw material for drug synthesis. A spiro compound N,N’-(2-oxo-3’H-spiro[indoline-3,2’-[1,3,4] thiadiazole]-3’5’-diyl)diacetamide were synthesise by refluxing Isatin And thiosemicarbazone in ethanol and then on heating with acetic anhydride underwent to cyclization into intermediate that on acetylation of the NH and NH2 groups afforded the spiro compound.
Słowa kluczowe
Rocznik
Tom
Strony
119--125
Opis fizyczny
Bibliogr. 31 poz., wykr., wz.
Twórcy
autor
- The Institute of Science, 15 Madam Cama Road, Fort, Mumbai - 400032, Maharastra, India
autor
- The Institute of Science, 15 Madam Cama Road, Fort, Mumbai - 400032, Maharastra, India
Bibliografia
- [1] E. Abele, R. Abele, O. Dzenibs, Chemistry of Hetrocylic Compounds 39(1) (2003)
- [2] E. G. Mesropyan, G. B. Ambrtsumyan, A. A. Avetisyan, Russian Journal Org. Chem. 39(8) (2003) 1130.
- [3] M. N. Zemtsova, P. L. Trakhtenborg, Russian Journal Org. Chem. 38 (2003) 1803.
- [4] Bespalova Zh. P., Lipkin A. E., Khim.-Farm. Zh., 1970, p. 24.
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- [7] W. Pfitzinger, J. Prakt. Chem. 33(2) (1886) 100.
- [8] R. Elderfield (editor), Heterocyclic Compounds 3 (1954) 164, (in Russian).
- [9] R. Elderfield (editor), Heterocyclic Compounds 4 (1955) 36, (in Russian).
- [10] Shtiintsa Kishinev, Isatin and its Derivatives, 1977, p. 228, (in Russian).
- [11] F. D. Popp, Adv. Heterocycl. Chem. 18 (1975) 2.
- [12] Joaquim F. M. da Silva, Simon J. Garden, Angelo C. Pinto, Journal of Brajil. Chem. Society 12(3) (2001) 273-324.
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- [14] Tatsungi J., Ikuma K., Izawa Y., Heterocycles 43 (1966) 7.
- [15] Tatsungi J., Hara T., Izawa Y., Chem. Let. (1977) 177.
- [16] Xue J., Zhang Y., Wang X-I., Fun H. K., Xu J-H., Org. Lett. 2 (2000) 2538.
- [17] Nair V., Sheela K. C., Rath N. P., Chem. Lett. (2000) 980.
- [18] Klumpp D. A., Yeung K. Y., Prakash G. K. S., Olah G. A., J. Org. Chem. 63 (1998) 4481.
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- [20] Garden S. J., Torres J. C., Ferreira A. A., Silva R. B., Pinto A. C., Tetrahedron Lett. 38 (1977) 1501.
- [21] Tatsungi J., Izawa Y., Synth. Commun. 28 (1988) 859.
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- [24] Gassmen P. G., Cue Jr. B. W., Luth T-Y, J. Org. Chem. 42 (1977) 1344.
- [25] N. Pandeya, P. Yogeeswari, J. P. Stables, Eur. J. Med. Chem. 35 (2000) 879-886.
- [26] S. N. Pandeya, B. Mishra, P. N. Singh, D. C. Rupainwar, Pharmacol. Res. 37(1998) 17-22.
- [27] M. Vermaet, Acta Pharm. 54 (2004) 49-56.
- [28] S. N. Pandeya, H. Manjula, J. P. Stables, Pharmazie 56 (2001) 121-124.
- [29] S. N. Pandeya, V. Mishra, I. Ponnilavarasan, J. P. Stables, Pol. J. Pharmacol 52 (2000) 283-290.
- [30] S. N. Pandeya, A. S. Raja, J. P. Stables, J. Pharm. Pharm. Sci. 5 (2002) 275-280.
- [31] Ratnamala P. Sonawane, Rahul R. Tripathi, Intrenational Letters of Chemistry, Physics and Astronomy 7(1)(2013) 30-36.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-b61365f2-9023-446e-8c51-76b79013b77d