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Synthesis of 1‐arylacenaphtho[1,2‐ d ]pyrazoles and 5,7‐Dehydro‐5 H ,7 H ‐benzo[ b ]acenaphtho[1,2‐ e ]‐1,3a,6a‐triazapentalenes
Author(s) -
Tsuge Otohiko,
Hatta Taizo,
Kojima Hisashi,
Miyahara Nobutaka,
Sugaya Masafumi
Publication year - 1994
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570310529
Subject(s) - chemistry , medicinal chemistry , stereochemistry
2‐Benzoyl‐ 5 and 2‐acetylacenaphthenone 6 , prepared from the corresponding 1‐acyl‐2‐(1‐pyrrolidinyl)‐acenaphthylenes 2 and 3 , reacted with arylhydrazines 8 under acidic conditions to give the corresponding 1‐arylacenaphtho[1,2‐ d ]pyrazoles 9 and 10 . Novel heteropentalene mesomeric betaines, 5,7‐dehydro‐5 H ,7 H ‐benzo[ b ]acenaphtho[1,2‐ e ]‐1,3a,6a‐triazapentalenes 13 and 14 were prepared by reductive cyclization of 1‐( o ‐nitrophenyl)acenaphtho[1,2‐ d ]pyrazoles 9d and 10d , respectively.

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