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Volumn 9, Issue 10, 2004, Pages 849-859

Unexpected hydrazinolysis behaviour of 1-chloro-4-methyl-5H-pyridazino[4,5- b]indole and a convenient synthesis of new [1,2,4]-triazolo[4′,3′:1, 6]pyridazino[4,5-b]indoles

Author keywords

Indole; Oxidative dehydrazination; Pyridazine; Triazole

Indexed keywords

1 CHLORO 4 METHYL 5H PYRIDAZINO[4,5 B]INDOLE; 3 ETHYL 6 METHYL 7H [1,2,4]TRIAZOLO[4',3':1,6]PYRIDAZINO[4,5 B]INDOLE; 3,6 DIMETHYL 7H [1,2,4]TRIAZOLO[4',3':1,6]PYRIDAZINO[4,5 B]INDOLE; 4 [2 [(6 METHYL 7H [1,2,4]TRIAZOLO[4',3':1,6]PYRIDAZINO[4,5 B]INDOL 3 YL)SULFANYL]ETHYL]MORPHOLINE; 6 METHYL 2,7 DIHYDRO 3H [1,2,4]TRIAZOLO[4',3':1,6]PYRIDAZINO[4,5 B]INDOL 3 ONE; 6 METHYL 2,7 DIHYDRO 3H [1,2,4]TRIAZOLO[4',3':1,6]PYRIDAZINO[4,5 B]INDOL 3 THIONE; 6 METHYL 3 (2 PHENYLETHYL) 7H [1,2,4]TRIAZOLO[4',3':1,6]PYRIDAZINO[4,5 B]INDOLE; 6 METHYL 3 PHENYL 7H [1,2,4]TRIAZOLO[4',3':1,6]PYRIDAZINO[4,5 B]INDOLE; 6 METHYL 7H [1,2,4]TRIAZOLO[4',3':1,6]PYRIDAZINO[4,5 B]INDOLE; ETHYL 6 METHYL 7H [1,2,4]TRIAZOLO[4',3':1,6]PYRIDAZINO[4,5 B]INDOLE 3 CARBOXYLATE; ETHYL(6 METHYL 7H [1,2,4]TRIAZOLO[4',3':1,6]PYRIDAZINO[4,5 B]INDOL 3 YL)ACETATE; HYDRAZINE; HYDRAZINE DERIVATIVE; INDOLE DERIVATIVE; INERT GAS; N,N DIETHYL N [2 [(6 METHYL 7H [1,2,4]TRIAZOLO[4',3':1,6]PYRIDAZINO[4,5 B]INDOL 3 YL)SULFANYL]ETHYL]AMINE; UNCLASSIFIED DRUG; [1,2,4]TRIAZOLO[4',3':1,6]PYRIDAZINO[4,5 B]INDOLE DERIVATIVE;

EID: 12344327758     PISSN: 14203049     EISSN: None     Source Type: Journal    
DOI: 10.3390/91000849     Document Type: Article
Times cited : (15)

References (13)
  • 3
    • 12344321767 scopus 로고
    • Stroh, R., Ed.; Thieme: Stuttgart
    • For an overview, cf. Enders, E. In Houben-Weyl Methoden der Organischen Chemie; Stroh, R., Ed.; Thieme: Stuttgart, 1967; Vol. 10/2, pp. 498-502.
    • (1967) Houben-Weyl Methoden der Organischen Chemie , vol.10 , Issue.2 , pp. 498-502
    • Enders, E.1
  • 11
    • 84993873348 scopus 로고
    • US Pat. 4728355, 1988
    • Henrie, R. N. US Pat. 4728355, 1988 [Chem. Abstr. 1988, 109, 33858].
    • (1988) Chem. Abstr. , vol.109 , pp. 33858
    • Henrie, R.N.1
  • 12
    • 85039470683 scopus 로고    scopus 로고
    • note
    • The formation of small amounts of side products bearing the alkyl side chain at position 7 was observed in both cases.
  • 13
    • 85039463299 scopus 로고    scopus 로고
    • note
    • 1H-NMR.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.