Phthalimidomethylthiadiazole

Phthalimidomethylthiadiazole

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  Chemistry and MaterialsResearch www.iiste.org ISSN 2224- 3224 (Print) ISSN 2225- 0956 (Online) Vol 1, No.1, 2011 Use of 5-[2-Ethoxyquinazolone-3-yl]-2- phthalimidomethylthiadiazole in the Synthesis of N- and C- Glycosides via Amadori Rearrangement Khalid M Darwish Chemistry Department, Science Faculty, University of Garyounis, Benghazi-Libya, E-mail: [email protected] Abstract Synthesis of novel 5-[2- aminoquinazolin-4-one-3-yl]-2- phthalimidomethylthiadiazole 2 from 5-[2-ethoxyquinazolin-4-one-3-yl]-2-phthalamidomethylthiadiazole 1. The behavior of 2 as a nitrogen nucleophile towards an α-hydroxy-aldehyde, such as glucose and formation of Amadori rearrangement product (ARP) 8 that has had occurred during the course of reaction was discussed. Keywords: N-Glycosides, α-bromoglucose, Amadori rearrangement, quinazolinone 1. Introduction In recent years there has been an increasing interest in the chemistry of 4(3H)-quinazolinone derivatives because of their biological importance. Many of them show antifungal (Partoli et al 1998), antibacterial (Abdel-Hamid et al 1997), anticancer (Barker 1995), anti-inflammatory (Bakhit et al 1998), anticonvulsant (Gursoy et al 1995), immunotropic (Nawrocka et al 1997), hypolipidemic (Kuroji et al 1996), antitumor (Hame et al 1996), antiulcer (Terashima et al 1995), analgesic (Hemalatha et al 2011), antiproliferative (Raffa et al 1999) activities and inhibitory effects for the thymidylate synthase and poly (ADP-ribose) polymerase (PARP) (Baek et al 1998). Some of 4- anilinoquinazolines have been found to be potential and highly selective inhibitors of human immunoglobulin E (Berger et al 2001) and epidermal growth factor receptor tyrosine kinase (Bridges 2001) which regulates the cell growth and proliferation, so they can work as potent anti- allergic or anti-cancer agents, respectively. 2. Results and Discussion It is well known that cyclic and acyclic nucleosides often enhance the biological activity of heterocyclic derivatives (Wang et al 2010). Herein we synthesized a novel 5-[2- aminoquinazolin-4-one-3-yl]-2-phthalimidomethylthiadiazole from our previously reported biologically active quinazolinone 5-[2-ethoxy-quinazolin-4-one-3-yl]-2- phthalamidomethylthiadiazole (El-Hashash et al 2011), and then discussed and reported its behavior as nitrogen nucleophile towards an α-hydroxy-aldehyde, such as glucose. In this paper, it is so important to pay attention to the so-called Amadori rearrangement that has had occurred during the course of reaction. The Amadori reaction, which is the first step in “Maillard browning” (Maillard 1912, Ibid 1912, Ledl et al 1990), is a potential non-enzymatic way to link reducing carbohydrates to complex biomolecules with reactive amino groups. The Amadori-rearrangement involves the reaction of α-hydroxy-aldehydes with suitable amine leading to the corresponding glycosylamine and the following rearrangement to the corresponding ketosamine, i.e. the Amadori-rearrangement product (ARP). The early mechanism for the Amadori-rearrangement was suggested by Kuhn and Weygand (1937). The initial reaction between the anomeric position of glucose and amino group of derivative 2 leads to the formation of glycosylamine 3 (Figure 1). After the protonation the Schiff base 5 is formed by ring opening, which is in equilibrium with the enol 6. This enol is stabilized by the formation of 1-amino-1-deoxyketohexose 7, which undergoes ring closure to the corresponding hemiketal 8. 8|Page www.iiste.org
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  Chemistry and MaterialsResearch www.iiste.org ISSN 2224- 3224 (Print) ISSN 2225- 0956 (Online) Vol 1, No.1, 2011 O O N N O S O S OH N O O a N b O N HO N N N HO OH NH N OCH 2CH 3 N NH H Q 1 2 3 (a) HCONH2 ; (b) glucose Q H Q H + Q H N H Q N H H N H H OH H OH O HO OH HO OH H H HO H NH Q H H HO O O H OH HO OH H OH OH H OH OH OH NH.HCl OH OH OH H OH Q OH 4 OH 8 7 6 5 Figure 1: Synthesis of the Amadori rearragement product 8 3. Experimental: General All melting points recorded are uncorrected. The IR spectra were recorded on a Pye Unicam SP 1200 spectrophotometer using the KBr wafer technique. The 1H-NMR spectra were determined on a Varian FT-200, or Bruker AC-200 MHz instrument using TMS as an internal standard. The chemical shifts (δ) are expressed in ppm. The mass spectra were determined using MP model NS-5988 and Shimadzu single focusing mass spectrometer (70 eV). All solvents used were of HPLC/AnalaR grade. All reagents were used as received from Alfa Aesar. Synthesis of Compounds 2, 3 and 8 A mixture of equimolar amounts of 5-[2-ethoxyquinazolin-4(3H)-one-3-yl]-2- phthalimidomethylthiadiazole 1 and formamide (0.01 mol) was heated under reflux for 5 h. The mixture was cooled and then poured onto ice/water with frequent stirring. The brown solid that separated out was filtered, washed with water, dried and crystallized from DMF to afford 2. Stirring derivative 2 (0.01 mol) with glucose (3 equivalents) in methanol (25 mL) at 40 oC for 12 h afforded brownish white syrupy solid of derivative 3. Protonation of derivative 3 was achieved by washing with an equimolar quantity of dilute hydrochloric acid (0.01 mol), affording light brown precipitate of 4 as the hydrochloride form. The presence of halogen was verified by a green flame with a copper wire. Treatment of product 4 with sodium bicarbonate solution (0.01 mol each) produced a dark brown precipitate which was filtered, washed frequently with water, dried and then crystallized with DMF affording derivative 8. Purification and separation of 8 was achieved using column chromatography (3:1 EtOAc: Hexane). 5-[2-Aminoquinazolin-4(3H)-one-3-yl]-2-phthalamidomethylthiadiazole 2: Brown crystals from DMF; m.p. 303-304 ºC; yield 85%. Anal. for C19H12N6O3S (m.w. 404): found: C, 56.55; H, 2.99; N, 20.84; S, 7.99; Calcd: C, 56.44; H, 2.97; N, 20.79; S, 7.92. IR υ (cm-1) 1631 (C=N), 1670, 1727, 1776 (3xC=O). MS: m/z (int. %) [M+H]+ 404 (58.0), 435 (22.8), 245 (36.4), 247 (3.4), 191(100), 193 (56.1), 186 (78.0), 188 (12.7), 175 (30.1), 177 (8.1), 157 (3.2), 159 (0.1), 147 (8.3), 149 (0.3), 130 (48.3), 132 (6.4), 122 (4.5), 124 (0.2), 78 (0.3), 80 (0.1);1H-NMR (DMSO-d6) δ 5.16 (s, 2H; CH2, 9|Page www.iiste.org
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  Chemistry and MaterialsResearch www.iiste.org ISSN 2224- 3224 (Print) ISSN 2225- 0956 (Online) Vol 1, No.1, 2011 phthalimidomethyl), 7.32-7.86 (m, 4H, quinazolinone), 7.94-8.03 (m, 4H, phthalimido-H), 9.38(bs, 1H, NH). 2-{[(3S, 5S)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]amino}quinazolin-4(3 H)-one 3: Brownish white syrupy solid from methanol; m.p. ˃ 300 oC; yield 80%. Anal. for C25H22N6O8S (m.w. 566): found: C, 56.48; H, 3.01; N, 20.83; S, 7.96; Calcd: C, 56.44; H, 2.97; N, 20.79; S, 7.92. IR υ (cm-1) 1634 (C=N), 1671, 1724, 1776 (3xC=O). 3-(5-Phthalimidomethyl-1,3,4-thiadiazol-2-yl)-2-{[(2,3,4,5-tetrahydroxytetrahydro-2H-pyran-2-yl)methyl) amino} quinazolin-4(3H)-one 8: Brown crystals from DMF; m.p. 303-304 ºC; yield 85 %. Anal. for C25H22N6O8S (m.w. 566): found: C, 53.06; H, 3.98; N, 14.92; S, 5.72; Calcd: C, 53.0; H, 3.93; N, 14.84; S, 5.65. IR υ (cm-1) 1631 (C=N), 1670, 1727, 1776 (3xC=O). MS: m/z (int. %) [M+H]+ 566 (58.0), 568 (22.8), 245 (36.4), 247 (3.4), 191 (100), 193 (56.1), 186 (78.0), 188 (12.7), 175 (30.1), 177 (8.1), 157 (3.2), 159 (0.1), 147 (8.3), 149 (0.3), 130 (48.3), 132 (6.4), 122 (4.5), 124 (0.2), 78 (0.3), 80 (0.1); 1H-NMR (DMSO-d6) δ 3.19 (dd, 1H, pyran-H-4), 3.28 (d, 1H, pyran-H-3), 3.55 (m, 1H, pyran-H-5), 3.72 (s, 2H, NHCH2), 3.81, 3.87 (2 dd, 2H, pyran-H-6a,b), 5.17 (s, 2H, phthalimido-CH2), 7.31-7.75 (m, 4H, quinazolinone), 7.72-7.88 (m, 4H, phthalimido-H), 9.42 (br s, 1H, NH). Acknowledgement The author wishes to express his gratitude to the chemistry department of Ain - Shams University for providing the research assistance for carrying out the pilot project. References and Notes Bartroli, J., Turmo, E., Alguero, M., Boncompte, E., Vericat, M.L., Coute, L., Ramis, J., Merlos, M., Garcia-Rafanell, J. & Forn, J. (1998), “New Azole Antifungals. 3. Synthesis and Antifungal Activity of 3-Substituted-4(3H)-quinazolinones”, J. Med. Chem. 41, 1869–82. Abdel-Hamid, S.G. (1997), “Synthesis of some New Heterocyclic Systems Bearing 2-Phenyl-6- iodo-4-(3H)-quinazolinon-3-yl Moiety as Antibacterial Agents”, J. Ind. Chem. Soc., 74, 613-618. Barker, A. (1995), “Preparation of 4-Anilinoquinazolines as Anticancer Agents”, J. Eur. Pat. 1995, 635498, Chem. Abstr. 122, 214099. Bekhit, A.A. & Khalil, M.A. (1998), “A Non-steroidal Anti-inflammatory Agents: Synthesis of Novel Benzopyrazolyl and Quinazolinyl Derivatives of 4(3H)-Quinazolinones”, Pharmazie, 53, 539- 543. Gursoy, A. & Karali, N. (1995), “Synthesis and Anticonvulsant Activity of New Acylthiosemicarbazides and Thiazolidone”s, Farmaco, 50, 857-866. Nawrocka, W. & Zimecki, M. (1997), “Syntheses of novel 3-amino-2(1H)-thioxo-4(3H)- quinazolinones and evaluation of their immunotropic activity. Part III”, Arch. Pharm., 330, 399- 405. Kurogi, Y., Inoue, Y., Tsutsumi, K., Nakamura, S., Nagao, K., Yoshitsugu, H. & Tsuda, Y. (1996), “Synthesis and hypolipidemic activities of novel 2-[4- [diethoxyphosphoryl)methyl]phenyl]quinazolines and 4(3H)-quinazolinones”, J. Med. Chem. 39(7), 1433-1437. Hame E., Lin C.M., Plowman, J., Wang, H.K., Lee, K.H. & Paull, K.D.(1996), “Antitumor 2,3- dihydro-2-(aryl)-4(1H)-quinazolinone derivatives: Interactions with tubulin”, Biochem. Pharmacol., 51, 51, 53-59. 10 | P a g e www.iiste.org
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  Chemistry and MaterialsResearch www.iiste.org ISSN 2224- 3224 (Print) ISSN 2225- 0956 (Online) Vol 1, No.1, 2011 Terashima, K., Shimamura, H., Kawase, A., Tanaka, Y., Tanimura, T., Kamisaki, T., Ishizuka, Y. & Sato, M. (1995), “Studies on Antiulcer Agents. IV. Antiulcer Effects of 2-Benzylthio-5,6,7,8- tetrahydro-4(3H)-quinazolinones and Related Compounds”, Chem. Pharm. Bull. 43, 2021-2023. Hemalatha, K. & Girija, K. (2011), “Synthesis of some novel 2,3-disubstituted quinazolinone derivatives as analgesic and anti-inflammatory agents”, 3(2), 103-106. Raffa, D., Dailone, G., Maggio, B., Sehillaci, D. & Plescia, F. (1999), “Synthesis and Antiproliferative Activity of Novel 3-(Indazol-3-yl)-quinazolin-4(3H)-one and 3-(Indazol-3-yl- benzotriazin-4(3H)-one Derivatives”, Arch. Pharm. 332, 317-320. Baek, D.J., Park, Y.K., Heo, H.I., Lee, M.H., Yang, Z.Y. & Chio, M.H. (1998), “Synthesis of 5- substituted quinazolinone derivatives and their inhibitory activity in vitro”, Bioorg. Med. Chem. Lett. 8, 3287-3290. Berger, M., Albrecht, B., Breces, A., Neruda, W. & Woisetschläger, M. (2001), “S(+)-4-(1- Phenyl- ethylamino)quinazolines as Inhibitors of Human Immunoglobuline E Synthesis: Potency is dictated by stereochemistry and atomic point charges at N-1”, J. Med. Chem. 44, 3031. Bridges, A.J. (2001), “Chemical inhibitors of protein kinases”, Chem. Rev. 101, 2541. Wang, L., Ankati, H., Akubathini, S.K., Balderamos, M., Storey, C.A., Patel, A.V., Price, V., Kretzschmar, D., Biehl, E.R. & D'Mello, S.R. (2010), “Identification of novel 1,4-benzoxazine compounds that are protective in tissue culture and in vivo models of neurodegeneration”, J. Neurosci Res. 88, 1970-1984. El-Hashash, M.A., Darwish, K.M., Rizk, S.A. & El-Bassiouny, F.A. (2011), “The Uses of 2- Ethoxy(4H)-3,1-benzoxazin-4-one in the Synthesis of Some Quinazolinone Derivatives of Antimicrobial Activity”, Pharmaceuticals, 4, 1032-1051. Maillard, L.C. (1912), C R Acad. Sci. Ser. 2, 154, 66. Ibid. (1912), 155, 1554. Ledl, F. & SSchleicher, E. (1990) Angew. Chem. 102, 597 and references cited therein. Kuhn, R. & Weygand, F. (1937), Ber., 70, 769. 11 | P a g e www.iiste.org