Investigation of the reaction products of 5‐amino‐1,3‐disubstituted‐pyrazoles with aromatic aldehydes. synthesis of new fluorinated 1,3,4‐trisubstituted‐4 H ‐pyrazolo[3,4‐ e ][1,4]thiazepin‐7‐ones | Zendy

Joshi Krishna C. | Zendy; Pathak Vijai N. | Zendy; Garg Urmila | Zendy

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Investigation of the reaction products of 5‐amino‐1,3‐disubstituted‐pyrazoles with aromatic aldehydes. synthesis of new fluorinated 1,3,4‐trisubstituted‐4 H ‐pyrazolo[3,4‐ e ][1,4]thiazepin‐7‐ones

Author(s) -

Joshi Krishna C.,

Pathak Vijai N.,

Garg Urmila

Publication year - 1980

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.5570170434

Subject(s) - chemistry , imine , condensation , organic chemistry , medicinal chemistry , condensation reaction , catalysis , physics , thermodynamics

The condensation products of 5‐amino‐1,3‐disubstituted‐pyrazoles with aromatic aldehydes were identified as 2,4‐dihydro‐2,5‐diphenyl‐4‐(phenylmethylene)‐3 H ‐pyrazol‐5‐imine derivatives Treatment of these products with mercaptoacetic acid gave new fluorine containing 1 H ‐pyrazolo[3,4‐ e ][1,4]thiazepin‐7‐ones.

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