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Volumn 50, Issue 27, 2009, Pages 3966-3969

A one-pot synthesis of 3,3′-methylenebis(2-arylamino-4H-chromen-4-one) from C-(4-oxo-4H-1-benzopyran-3-yl)-N-arylnitrone

Author keywords

1 Benzopyran; 3 Formylchromone; Bischromones; Deformylation; Mannich reaction; Nitrones

Indexed keywords

12H CHROMENO[2,3 B]QUINOLIN 12 ONE; AMINE; CHROMENE DERIVATIVE; DIETHYLAMINE; FORMALDEHYDE; PIPERIDINE; QUINOLINE DERIVATIVE; SARCOSINE; UNCLASSIFIED DRUG;

EID: 65549133717     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.04.087     Document Type: Article
Times cited : (13)

References (25)
  • 9
    • 22444437129 scopus 로고
    • Weisberger A. (Ed), Interscience, New York Chapter XXI, and references therein
    • Ellis G.P. In: Weisberger A. (Ed). Heterocyclic Compounds Vol. 31 (1977), Interscience, New York 1043-1083 Chapter XXI, and references therein
    • (1977) Heterocyclic Compounds , vol.31 , pp. 1043-1083
    • Ellis, G.P.1
  • 24
    • 65549091712 scopus 로고    scopus 로고
    • note
    • ++Na).
  • 25
    • 65549111027 scopus 로고    scopus 로고
    • note
    • 2 = aryl) (1 mmol) was heated under reflux in ethanol (25 mL) for 2 h and complete conversion of 2 to 3 was observed by TLC. Under this condition, piperidine (85 mg, 1 mmol) and 37% aqueous formaldehyde solution (1.5 mL) were added to the reaction mixture and heated under reflux for another 3 h, when a white solid separated out. The solid was filtered and crystallized from benzene-petroleum ether (10:1) to afford 8 in 80-90% yields.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.