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Volumn 36, Issue 19, 2006, Pages 2797-2805

Synthesis of the 7-azaindole (1H-pyrrolo[2,3-b]pyridine) analogous to cannabimimetic JHW 200

Author keywords

7 azaindole; Amino alkyl indole; Cannabimimetic; Grignard condensation

Indexed keywords

1 NAPHTHYL MAGNESIUM BROMIDE; 2,3 DIHYDRO 5 METHYL 3 (MORPHOLINOMETHYL) 6 (1 NAPHTHOYL)PYRROLO[1,2,3 DE][1,4]BENZOXAZINE; 7 AZAINDOLE DERIVATIVE; BROMINE DERIVATIVE; CANNABINOID; DF 1012; INDOLE DERIVATIVE; JHW 200; MAGNESIUM DERIVATIVE; NITRILE; TETRAHYDROCANNABINOL; UNCLASSIFIED DRUG; [1 (2 MORPHOLIN 4 YL ETHYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL]NAPHTHALEN 1 YL METHANONE;

EID: 33750089733     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910600767504     Document Type: Article
Times cited : (4)

References (19)
  • 2
    • 33947489961 scopus 로고
    • Isolation, structure and partial synthesis of an active constituent of hashish
    • Gaoni, Y.; Mechoulam, R. Isolation, structure and partial synthesis of an active constituent of hashish. J. Am. Chem. Soc. 1964, 86, 1648-1649.
    • (1964) J. Am. Chem. Soc. , vol.86 , pp. 1648-1649
    • Gaoni, Y.1    Mechoulam, R.2
  • 4
    • 1642543378 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 1,8-naphthyridin-4(1H)-on-3- carboxamide derivatives as new ligands of cannabinoid receptors
    • Ferrarini, P. L.; Calderone, V.; Cavallini, T.; Manera, C.; Saccomani, G.; Pani; Ruiu, S.; Gessa, G. L. Synthesis and biological evaluation of 1,8-naphthyridin-4(1H)-on-3-carboxamide derivatives as new ligands of cannabinoid receptors. Bioorg. Med. Chem. 2004, 12, 1921-1933.
    • (2004) Bioorg. Med. Chem. , vol.12 , pp. 1921-1933
    • Ferrarini, P.L.1    Calderone, V.2    Cavallini, T.3    Manera, C.4    Saccomani, G.5    Pani6    Ruiu, S.7    Gessa, G.L.8
  • 5
    • 0037248374 scopus 로고    scopus 로고
    • 3-Indolyl-1-naphtylmethanes: New cannabimimetic indoles provide evidence for aromatic stacking interactions with the CB1 cannabinoid receptor
    • Huffman, J. W.; Mabon, R.; Wu, M.-Y.; Lu, J.; Hart, R.; Hurst, D. P.; Reggio, P. H.; Willey, J. L.; Martin, B. R. 3-Indolyl-1-naphtylmethanes: New cannabimimetic indoles provide evidence for aromatic stacking interactions with the CB1 cannabinoid receptor. Bioorg. Med. Chem. 2003, 11, 539-549.
    • (2003) Bioorg. Med. Chem. , vol.11 , pp. 539-549
    • Huffman, J.W.1    Mabon, R.2    Wu, M.-Y.3    Lu, J.4    Hart, R.5    Hurst, D.P.6    Reggio, P.H.7    Willey, J.L.8    Martin, B.R.9
  • 7
    • 0032451280 scopus 로고    scopus 로고
    • Brain cannabinoid systems as targets for the therapy of neurological disorders
    • Consroe, P. Brain cannabinoid systems as targets for the therapy of neurological disorders. Neurobiol Dis. 1998, 5, 534-551.
    • (1998) Neurobiol Dis. , vol.5 , pp. 534-551
    • Consroe, P.1
  • 8
    • 0036278032 scopus 로고    scopus 로고
    • Targetting the endocannabinoid system in cancer therapy: A call for further reaseach
    • Bifulco, M.; Di Marzo, V. Targetting the endocannabinoid system in cancer therapy: A call for further reaseach. Nat. Med. 2002, 8, 547-550.
    • (2002) Nat. Med. , vol.8 , pp. 547-550
    • Bifulco, M.1    Di Marzo, V.2
  • 10
    • 0037997585 scopus 로고    scopus 로고
    • Synthesis and reactivity of 7-azaindoles (1H-pyrrolo[2,3-b] pyridine)
    • Merour, J.-Y.; Joseph, B. Synthesis and reactivity of 7-azaindoles (1H-pyrrolo[2,3-b] pyridine). Curr. Org. Chem. 2001, 5, 471-506.
    • (2001) Curr. Org. Chem. , vol.5 , pp. 471-506
    • Merour, J.-Y.1    Joseph, B.2
  • 11
    • 0038065535 scopus 로고    scopus 로고
    • Synthesis of isogranulatinides A and B analogues possessing a 7-azaindole unit instead of an indole moiety
    • Hugon, B.; Pfeiffer, B.; Renard, P.; Prudhomme, M. Synthesis of isogranulatinides A and B analogues possessing a 7-azaindole unit instead of an indole moiety. Tetrahedron Lett. 2003, 44, 4607-4611.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 4607-4611
    • Hugon, B.1    Pfeiffer, B.2    Renard, P.3    Prudhomme, M.4
  • 12
    • 2442687670 scopus 로고    scopus 로고
    • Synthesis of a staurosporine analogue possessing a 7-azaindole unit instead of a indole moiety
    • Messaoudi, S.; Anizon, F.; Pfeiffer, B.; Goldteyn, R.; Prudhomme, M. Synthesis of a staurosporine analogue possessing a 7-azaindole unit instead of a indole moiety. Tetrahedron Lett. 2004, 45, 4643-4647.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 4643-4647
    • Messaoudi, S.1    Anizon, F.2    Pfeiffer, B.3    Goldteyn, R.4    Prudhomme, M.5
  • 16
    • 0000135356 scopus 로고
    • 7-Azaindole, synthesis and conversion to 7-azatryptophan and other derivatives
    • Robinson, M.; Robinson, B. 7-Azaindole, synthesis and conversion to 7-azatryptophan and other derivatives. J. Am. Chem. Soc. 1955, 77, 457-460.
    • (1955) J. Am. Chem. Soc. , vol.77 , pp. 457-460
    • Robinson, M.1    Robinson, B.2
  • 17
    • 0033574716 scopus 로고    scopus 로고
    • A new method for the synthesis of ketones: The palladium-catalysed cross-coupling of acid chlorides with arylboronic acids
    • Haddach, M.; McCarty, J. R. A new method for the synthesis of ketones: The palladium-catalysed cross-coupling of acid chlorides with arylboronic acids. Tetrahedron Lett. 1999, 40, 3109-3112.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 3109-3112
    • Haddach, M.1    McCarty, J.R.2
  • 18
    • 0036798533 scopus 로고    scopus 로고
    • Palladium-catalysed synthesis of aryl ketones from boronic acids and carboxylic acids activated in situ by pivalic anhydride
    • Gooßen, L.J.; Ghosh, K. Palladium-catalysed synthesis of aryl ketones from boronic acids and carboxylic acids activated in situ by pivalic anhydride. Eur. J. Org. Chem. 2002, 3254-3267.
    • (2002) Eur. J. Org. Chem. , pp. 3254-3267
    • Gooßen, L.J.1    Ghosh, K.2
  • 19
    • 84985294285 scopus 로고
    • Reactivity of 1H-Pyrrolo[2,3-b]pyridine. Synthesis of 3 acetyl-7-azaindole and related compounds
    • Galvez, G.; Viladoms, P. Reactivity of 1H-Pyrrolo[2,3-b]pyridine. Synthesis of 3 acetyl-7-azaindole and related compounds. J. Heterocycl. Chem. 1982, 19, 665-667.
    • (1982) J. Heterocycl. Chem. , vol.19 , pp. 665-667
    • Galvez, G.1    Viladoms, P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.