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Volumn 64, Issue 11, 2008, Pages 2605-2610

A convenient microwave-assisted desulfitative dimethylamination of the 2(1H)-pyrazinone scaffold using N,N-dimethylformamide

Author keywords

2(1H) Pyrazinone; Desulfitative; Dimethylamination; DMF; Microwave assisted organic synthesis (MAOS)

Indexed keywords

1 (4 METHOXYBENZYL) 3 (N BENZYL N METHYLAMINO) 5 CHLOROPYRAZIN 2(1H) ONE; 1 (4 METHOXYBENZYL) 5 CHLORO 3 (DIMETHYLAMINO) 6 (4 METHOXYPHENYL)PYRAZIN 2(1H) ONE; 1 (4 METHOXYBENZYL) 5 CHLORO 3 (DIMETHYLAMINO)PYRAZIN 2(1H) ONE; 1 (4 METHOXYBENZYL) 5 CHLORO 3 (ISOBUTYLAMINO)PYRAZIN 2(1H) ONE; 1 (4 METHOXYBENZYL) 5 CHLORO 3 (PIPERIDIN 1 YL)PYRAZIN 2(1H) ONE; 1 (4 METHOXYBENZYL) 5 CHLORO 3 MORPHOLINOPYRAZIN 2(1H) ONE; 1 (4 METHOXYBENZYL) 6 BENZYL 5 CHLORO 3 (DIMETHYLAMINO)PYRAZIN 2(1H) ONE; 1 BENZYL 5 CHLORO 3 (DIMETHYLAMINO) 6 METHYLPYRAZIN 2(1H) ONE; 3 (DIMETHYLAMINO) 5 (PHENYLTHIO) 6 2 TOLYL 2H 1,4 OXAZIN 2 ONE; 5 CHLORO 1 (4 METHOXYBENZYL) 3 (PHENYLSULFANYL)PYRAZIN 2(1H) ONE; 5 CHLORO 1 (CYCLOHEXYLMETHYL) 3 (DIMETHYLAMINO)PYRAZIN 2(1H) ONE; 5 CHLORO 3 (DIMETHYLAMINO) 1 (3 PHENYLPROPYL)PYRAZIN 2(1H) ONE; 5 CHLORO 3 (DIMETHYLAMINO) 1 (4 METHOXYBENZYL)PYRAZIN 2(1H) ONE; 5 CHLORO 3 (DIMETHYLAMINO) 1 (4 METHOXYPHENYL)PYRAZIN 2(1H) ONE; 5 CHLORO 3 (DIMETHYLAMINO) 1,6 DIMETHYLPYRAZIN 2(1H) ONE; 5 CHLORO 3 (DIMETHYLAMINO)PYRAZIN 2(1H) ONE DERIVATIVE; 5 CHLORO 3 (PHENYLSULFANYL) 2(1H) ONE DERIVATIVE; KETONE DERIVATIVE; N,N DIMETHYLFORMAMIDE; OXAZINONE; SODIUM CARBONATE; UNCLASSIFIED DRUG;

EID: 38749120081     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.01.030     Document Type: Article
Times cited : (44)

References (37)
  • 1
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    • Buckingham J. (Ed), Chapman and Hall, London
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    • (1993) Dictionary of Natural products
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    • In: Buckingham J., and MacDonald F. (Eds). Dictionary of Organic Compounds (1996), Chapman and Hall, London
    • (1996) Dictionary of Organic Compounds
  • 3
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    • For detailed description, see review: and references cited therein;
    • For detailed description, see review:. Baloglu E., and Kingston D.G.I. J. Nat. Prod. 62 (1999) 1448-1472 and references cited therein;
    • (1999) J. Nat. Prod. , vol.62 , pp. 1448-1472
    • Baloglu, E.1    Kingston, D.G.I.2
  • 36
    • 38749093411 scopus 로고    scopus 로고
    • note
    • The GC-LRMS experiment was performed at 160 °C instead of 250 °C as routinely kept for all GC-LRMS experiments.
  • 37
    • 38749128036 scopus 로고    scopus 로고
    • note
    • ®). The crude mixture was evaluated with GC-LRMS at 180 °C. GC-MS analysis of pure DMF did not show any traces of dimethylamine clearly indicating in situ generation of dimethylamine under the conditions used.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.