메뉴 건너뛰기




Volumn 40, Issue 5, 2010, Pages 677-685

Sulfamic acid-catalyzed, three-component, one-pot synthesis of [1,2,4]Triazolo/benzimidazolo quinazolinone derivatives

Author keywords

2 Amino benzimidazole; 3 amino 1,2,4 triazole; Sulfamic acid; Triazolo benzimidazolo quinazolinones

Indexed keywords

12(4 BROMO PHENYL) 3,3 DIMETHYL 1,2,3,4,5,12 HEXAHYDROBENZO[4,5]IMIDAZO[2,1 B]QUINAZOLIN 1 ONE; 12(4 CHLOROPHENYL) 3,3 DIMETHYL 1,2,3,4,5,12 HEXAHYDROBENZO[4,5]IMIDAZO[2,1 B]QUINAZOLIN 1 ONE; 2 AMINO BENZIMIDAZOLE; 3,3 DIMETHYL 12 PHENYL 1,2,3,4,5,12 HEXAHYDROBENZO[4,5]IMIDAZO[2,1 B]QUINAZOLIN 1 ONE; 3,3 DIMETHYL 12(4 HYDROXY PHENYL) 1,2,3,4,5,12 HEXAHYDROBENZO[4,5]IMIDAZO[2,1 B]QUINAZOLIN 1 ONE; 3,3 DIMETHYL 12(4 METHOXY PHENYL) 1,2,3,4,5,12 HEXAHYDROBENZO[4,5]IMIDAZO[2,1 B]QUINAZOLIN 1 ONE; 3,3 DIMETHYL 12(4 NITRO PHENYL) 1,2,3,4,5,12 HEXAHYDROBENZO[4,5]IMIDAZO[2,1 B]QUINAZOLIN 1 ONE; 5,5 DIMETHYL 1,3 CYCLOHEXANEDIONE; 6,6 DIMETHYL 9 (4 HYDROXY PHENYL) 5,6,7,9 TETRAHYDRO 1,2,4 TRIAZOLO[5,1 B]QUINAZOLIN 8(4H) ONE; 6,6 DIMETHYL 9 (4 NITRO PHENYL) 5,6,7,9 TETRAHYDRO 4H 1,2,4 TRIAZOLO[5,1 B]QUINAZOLIN 8 ONE; 6,6 DIMETHYL 9(2 NAPHTHYL) 5,6,7,9 TETRAHYDRO 1,2,4 TRIAZOLO[5,1 B]QUINAZOLIN 8(4H) ONE; 6,6 DIMETHYL 9(3 NITRO- HENYL) 5,6,7,9 TETRAHYDRO 1,2,4 TRIAZOLO[5,1 B]QUINAZOLIN 8(4H) ONE; 6,6 DIMETHYL 9(4 METHOXY PHENYL) 5,6,7,9 TETRAHYDRO 4H 1,2,4 TRIAZOLO[5,1 B]QUINAZOLIN 8 ONE; 6,6 DIMETHYL 9(4 METHYL PHENYL) 5,6,7,9 TETRAHYDRO 4H 1,2,4 TRIAZOLO[5,1 B]QUINAZOLIN 8 ONE; 9 (4 BROMO PHENYL) 6,6 DIMETHYL 5,6,7,9 TETRAHYDRO 4H-1,2,4 TRIAZOLO[5,1 B]QUINAZOLIN 8 ONE; 9 (4 CHLORO PHENYL) 6,6 DIMETHYL 5,6,7,9 TETRAHYDRO 4H 1,2,4 TRIAZOLO[5,1 B]QUINAZOLIN 8 ONE; 9 PHENYL 6,6 DIMETHYL 5,6,7,9 TETRAHYDRO 4H 1,2,4 TRIAZOLO[5,1 B]QUINAZOLIN 8 ONE; [1,2,4]TRIAZOLO QUINAZOLINONE; ACETONITRILE; ALDEHYDE DERIVATIVE; AMITROLE; BENZIMIDAZOLE DERIVATIVE; BENZIMIDAZOLO QUINAZOLINONE; QUINAZOLINONE DERIVATIVE; SULFAMIC ACID; SULFAMIDE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 76349092462     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910903009489     Document Type: Article
Times cited : (87)

References (23)
  • 1
    • 0033775563 scopus 로고    scopus 로고
    • Pyrrole, pyrrolidine, pyridine, piperidine, and tropane alkaloids
    • Hagan, D. O. Pyrrole, pyrrolidine, pyridine, piperidine, and tropane alkaloids. Nat. Prod. Rep. 2000, 17, 435.
    • (2000) Nat. Prod. Rep. , vol.17 , pp. 435
    • Hagan, D.O.1
  • 3
    • 34047188045 scopus 로고    scopus 로고
    • Synthesis and antihypertensive activity of novel 3-benzyl-2-substituted- 3H-[1, 2,4]triazolo[5,1-b]quinazolin-9-ones
    • Alagarsamy, V.; Pathak, U. S. Synthesis and antihypertensive activity of novel 3-benzyl-2-substituted-3H-[1,2,4]triazolo[5,1-b]quinazolin-9-ones. Bioorg. Med. Chem. 2007, 15, 3457.
    • (2007) Bioorg. Med. Chem. , vol.15 , pp. 3457
    • Alagarsamy, V.1    Pathak, U.S.2
  • 4
    • 6344269995 scopus 로고    scopus 로고
    • Synthesis and pharmacological investigation of some novel 2-methyl-3-(substituted methylamino)-(3H)-quinazolin-4-ones as histamine H1-receptor blockers
    • Alagarsamy, V. Synthesis and pharmacological investigation of some novel 2-methyl-3-(substituted methylamino)-(3H)-quinazolin-4-ones as histamine H1-receptor blockers. Pharmazie 2004, 59, 753.
    • (2004) Pharmazie , vol.59 , pp. 753
    • Alagarsamy, V.1
  • 5
    • 10844248503 scopus 로고    scopus 로고
    • Synthesis analgesic, anti-inflammatory, and antibacterial activities of some novel 2-methyl-3-substituted quinazolin-4-(3H)-ones
    • Alagarsamy, V.; Murugananthan, G.; Venkateshperumal, R. Synthesis, analgesic, anti-inflammatory, and antibacterial activities of some novel 2-methyl-3-substituted quinazolin-4-(3H)-ones. Biol. Pharm. Bull. 2003,26, 1711.
    • (2003) Biol. Pharm. Bull. , vol.26 , pp. 1711
    • Alagarsamy, V.1    Murugananthan, G.2    Venkateshperumal, R.3
  • 6
    • 0034676319 scopus 로고    scopus 로고
    • 6-Alkylamino-and 2,3-dihydro-3-methoxy-2-phenyl-4-quinazolinones and related compounds: Their synthesis, cytotoxicity, and inhibition of tubulin polymerization
    • Hour, M. J.; Huang, L. J.; Kuo, S. C; Xia, Y.; Bastow, K.; Nakanishi, Y.; Hamel, E.; Lee, K. H. 6-Alkylamino-and 2,3-dihydro-3-methoxy-2-phenyl-4- quinazolinones and related compounds: Their synthesis, cytotoxicity, and inhibition of tubulin polymerization. J. Med. Chem. 2000, 43, 4479.
    • (2000) J. Med. Chem. , vol.43 , pp. 4479
    • Hour, M.J.1    Huang, L.J.2    Kuo, S.C.3    Xia, Y.4    Bastow, K.5    Nakanishi, Y.6    Hamel, E.7    Lee, K.H.8
  • 8
    • 0022669172 scopus 로고
    • Guanidine-annelated heterocycles, VII: Synthesis and antihypertensive activity of 2,10-dimethyl-5H,10H-1,2,4-triazolo[5,1-b]quinazolin-5-one
    • Liu, K. C; Hu, M. K. Guanidine-annelated heterocycles, VII: Synthesis and antihypertensive activity of 2,10-dimethyl-5H,10H-1,2,4-triazolo[5,1-b] quinazolin-5-one. Arch. Pharm. 1986, 319, 188.
    • (1986) Arch. Pharm. , vol.319 , pp. 188
    • Liu, K.C.1    Hu, M.K.2
  • 10
    • 0011984675 scopus 로고
    • E. Schumann (Ed.); Thieme: Stuttgart
    • Dhne, H. In Methoden der Organischen Chemie; E. Schumann (Ed.); Thieme: Stuttgart, 1994; vol.E8d, p. 305.
    • (1994) In Methoden der Organischen Chemie , vol.E8D , pp. 305
    • Dhne, H.1
  • 11
    • 84890597202 scopus 로고    scopus 로고
    • For a monograph, see Zhu J., Bienayme H. (Eds.) Wiley-VCH: Weinhein, Germany
    • For a monograph, see Zhu, J.; Bienayme, H. (Eds.). Multicomponent Reactions; Wiley-VCH: Weinhein, Germany, 2005.
    • (2005) Multicomponent Reactions
  • 12
    • 31544434530 scopus 로고    scopus 로고
    • Recent developments in isocyanide based multicomponent reactions in applied chemistry
    • Domling, A. Recent developments in isocyanide based multicomponent reactions in applied chemistry. Chem. Rev. 2006, 106, 17.
    • (2006) Chem. Rev. , vol.106 , pp. 17
    • Domling, A.1
  • 13
    • 33646069977 scopus 로고    scopus 로고
    • New multicomponent approach for the creation of chiral quaternary centers in the carbonyl allylation reactions
    • Sklute, G.; Marek, I. New multicomponent approach for the creation of chiral quaternary centers in the carbonyl allylation reactions. J. Am. Chem. Soc. 2006, 128, 4642.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 4642
    • Sklute, G.1    Marek, I.2
  • 15
    • 4544253640 scopus 로고    scopus 로고
    • Sulphamic acid: An efficient and cost-effective solid acid catalyst for the Pechmann reaction
    • Sing, P. R.; Singh, D. U.; Samant, S. D. Sulphamic acid: An efficient and cost-effective solid acid catalyst for the Pechmann reaction. Synlett 2004, 1909.
    • (2004) Synlett , vol.1909
    • Sing, P.R.1    Singh, D.U.2    Samant, S.D.3
  • 17
  • 18
    • 34248160897 scopus 로고    scopus 로고
    • A modified and green Dakin-West reaction: An efficient and convenient method for a one-pot synthesis of (5-acetamido carbonyl compounds
    • Heravi, M. M.; Ranjbar, L.; Derikvand, F.; Bamoharram, F. F. A modified and green Dakin-West reaction: An efficient and convenient method for a one-pot synthesis of (5-acetamido carbonyl compounds. J. Mol. Catal. A: Chem. 2007, 271, 28.
    • (2007) J. Mol. Catal. A: Chem. , vol.271 , pp. 28
    • Heravi, M.M.1    Ranjbar, L.2    Derikvand, F.3    Bamoharram, F.F.4
  • 19
    • 34249670726 scopus 로고    scopus 로고
    • Oxidative aromatization of Hantzsch 1,4-dihydropyridines in the presence of mixed-addenda vanadomolybdophosphate heteropolyacid, H6PMo9V3O40
    • Heravi, M. M.; Derikvand, F.; Hasanpour, S.; Bakhtiari, K.; Bamoharram, F. F.; Oskooie, H. A. Oxidative aromatization of Hantzsch 1,4-dihydropyridines in the presence of mixed-addenda vanadomolybdophosphate heteropolyacid, H6PMo9V3O40. Bioorg. Med. Chem. Lett. 2007, 17, 3305.
    • (2007) Bioorg. Med. Chem. Lett. , vol.17 , pp. 3305
    • Heravi, M.M.1    Derikvand, F.2    Hasanpour, S.3    Bakhtiari, K.4    Bamoharram, F.F.5    Oskooie, H.A.6
  • 20
    • 33847694320 scopus 로고    scopus 로고
    • Catalytic oxidative cleavage of C=N bond in the presence of mixed-addenda vanadomolybdophosphate, H6PMo9V3O40 as a green and reusable catalyst
    • Heravi, M. M.; Ranjbar, L.; Derikvand, F.; Oskooie, H. A.; Bamoharram, F. F. Catalytic oxidative cleavage of C=N bond in the presence of mixed-addenda vanadomolybdophosphate, H6PMo9V3O40 as a green and reusable catalyst. J. Mol. Catal. A: Chem. 2007, 265, 186.
    • (2007) J. Mol. Catal. A: Chem. , vol.265 , pp. 186
    • Heravi, M.M.1    Ranjbar, L.2    Derikvand, F.3    Oskooie, H.A.4    Bamoharram, F.F.5
  • 22
    • 1642528397 scopus 로고    scopus 로고
    • Synthesis of 9-aryl-6 6-dimethyl-5, 6, 7,9-tetrahydro-1,2,4-triazolo-[5, 1-b]quinazolin-8(4H)ones
    • Lipson, V. V.; Desenko, S. M.; Shirobokova, M. G.; Borodina, V. V. Synthesis of 9-aryl-6,6-dimethyl-5,6,7,9-tetrahydro-1,2,4-triazolo-[5,1-b] quinazolin-8(4H)ones. Chem. Het. Comp. 2003, 39, 1213.
    • (2003) Chem. Het. Comp. , vol.39 , pp. 1213
    • Lipson, V.V.1    Desenko, S.M.2    Shirobokova, M.G.3    Borodina, V.V.4
  • 23


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.