메뉴 건너뛰기




Volumn 38, Issue 31, 1997, Pages 5555-5558

New CNS agent precursors. A simple and efficient route for synthesis of 6-aminomethyl-4,5,6,7- tetrahydrobenzofuran-4-ones as conformationally constrained butyrophenone analogues

Author keywords

[No Author keywords available]

Indexed keywords

6 AMINOMETHYL 4,5,6,7 TETRAHYDROBENZOFURAN 4 ONE DERIVATIVE; BUTYROPHENONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0030753879     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)01242-2     Document Type: Article
Times cited : (10)

References (19)
  • 1
    • 0000615263 scopus 로고
    • Dopamine receptors
    • Hansch, C.; Sammes, P. G.; Taylor, J. B., Eds.; Pergamon Press: Oxford
    • Horu, A. S.; Dopamine receptors. In Comprehensive Medicinal Chemistry; Hansch, C.; Sammes, P. G.; Taylor, J. B., Eds.; Pergamon Press: Oxford, 1990; vol. 3, p. 133.
    • (1990) Comprehensive Medicinal Chemistry , vol.3 , pp. 133
    • Horu, A.S.1
  • 11
    • 0030592705 scopus 로고    scopus 로고
    • and references cited therein
    • Arylpiperazines are important tools in the field of Medicinal Chemistry. Every year, several new methods for the synthesis of such compounds are proposed. See Perez, M.; Potier, P.; Halazy, S. Tetrahedron Lett. 1996, 47, 8487-8488, and references cited therein.
    • (1996) Tetrahedron Lett. , vol.47 , pp. 8487-8488
    • Perez, M.1    Potier, P.2    Halazy, S.3
  • 12
    • 0017916143 scopus 로고
    • The 4-(p-fluorobenzoyl)piperidine fragment may be considered as a butyrophenone moiety constrained in a six-membered ring. The importance of this fragment on CNS agents acting compounds is well known. See, among others, (a) Boswell, R. F., Jr.; Welstead, W. J., Jr.; Duncan, R. L., Jr.; Johnson, D. N.; Funderburk, W. H. J. Med. Chem. 1978, 21, 136-138;
    • (1978) J. Med. Chem. , vol.21 , pp. 136-138
    • Boswell R.F., Jr.1    Welstead W.J., Jr.2    Duncan R.L., Jr.3    Johnson, D.N.4    Funderburk, W.H.5
  • 17
    • 0343970743 scopus 로고    scopus 로고
    • note
    • 4) and concentrated under reduced presure. Silica gel chromatography of the residue (hexane/ethyl acetate 1:4 as eluent) gave the alcohol 2 (0.63 g, 60%) as yellow oil.
  • 18
    • 0343098951 scopus 로고    scopus 로고
    • note
    • 2: C, 70.55%; H, 8.65%; N, 6.32. Found: C, 70.81; H, 8.64; N, 6.13.
  • 19
    • 0343970742 scopus 로고    scopus 로고
    • note
    • 13C-NMR, FTIR, MS). Yields given correspond to isolated pure compounds.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.