vilsmeier-haack reaction with 2,3,3-trimethyl-3h-benzo[g]indole and its conversion into 2-(1-aryl-1h-pyrazol-4-yl)-3,3-dimethyl-3h-benzo[g]indoles

Authors

mohsen khezri

department of organic chemistry, faculty of chemistry, university of urmia, urmia 57153-165, iran arash afghan

urmia university of technology, urmia, iran laya roohi

department of organic chemistry, faculty of chemistry, university of urmia, urmia 57153-165, iran mohammad mehdi baradarani

department of organic chemistry, faculty of chemistry, university of urmia, urmia 57153-165, iran

abstract

vilsmeier-haack reaction of 2,3,3-trimethyl-3h-benzo[g]indole, then aqueous basic work-up, leads to benzo[g]indol-2-ylidene- malondialdehydes. these react with various arylhydrazines and quinolin-2-ylhydrazine to form 3,3-dimethyl-2-(1-aryl-1h-pyrazol-4-yl)- 3h-benzo[g]indoles in good yields.

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Vilsmeier-Haack Reaction with 2,3,3-Trimethyl-3H-benzo[g]indole and Its Conversion into 2-(1-aryl-1H-pyrazol-4-yl)-3,3-dimethyl-3H-benzo[g]indoles

Vilsmeier-Haack reaction of 2,3,3-trimethyl-3H-benzo[g]indole, then aqueous basic work-up, leads to benzo[g]indol-2-ylidene- malondialdehydes. These react with various arylhydrazines and quinolin-2-ylhydrazine to form 3,3-dimethyl-2-(1-aryl-1H-pyrazol-4-yl)- 3H-benzo[g]indoles in good yields.

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Journal title:
organic chemistry research

جلد ۲، شماره ۲، صفحات ۱۲۰-۱۲۶

Keywords
[ ' v i l s m e i e r ' , ' h a a c k r e a c t i o n ' , ' f o r m y l a t i o n ' , ' p y r a z o l e ' , ' m a l o n d i a l d e h y d e ' , 2 , ' q u i n o l y l h y d r a z i n e ' , ' a r y l h y d r a z i n e ' ]

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