The title compound, C18H15N3O, is the product of the thermal decomposition of the diazo-nium salt derived from 2-amino-N-methyl-N-(3-methyl-1-phenyl-1H- pyrazol-5-yl)benzamide. It is characterized by a trans orientation of the methyl groups with respect to the tricyclic ring system. The mol-ecule has a nearly planar phenyl-pyrazolo[3,4-c]isoquinolin-5-one system, the largest deviation from the mean plane being 0.066 (2) Å for the O atom. The dihedral angle between the phenyl substituent and the heterotricycle is 67 (1)°. The packing is stabilized by C - H⋯N hydrogen-bond inter-actions, with the formation of mol-ecular chains along the c axis.

1,4-dimethyl-3-phenyl-3H-pyrazolo[3,4-c]isoquinolin-5(4H)-one / F. Meneghetti, G. Bombieri, G. Daidone, B. Maggio. - In: ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE. - ISSN 1600-5368. - 64:5(2008), p. O863-U2109.

1,4-dimethyl-3-phenyl-3H-pyrazolo[3,4-c]isoquinolin-5(4H)-one

F. Meneghetti
Primo
;
G. Bombieri
Secondo
;
2008

Abstract

The title compound, C18H15N3O, is the product of the thermal decomposition of the diazo-nium salt derived from 2-amino-N-methyl-N-(3-methyl-1-phenyl-1H- pyrazol-5-yl)benzamide. It is characterized by a trans orientation of the methyl groups with respect to the tricyclic ring system. The mol-ecule has a nearly planar phenyl-pyrazolo[3,4-c]isoquinolin-5-one system, the largest deviation from the mean plane being 0.066 (2) Å for the O atom. The dihedral angle between the phenyl substituent and the heterotricycle is 67 (1)°. The packing is stabilized by C - H⋯N hydrogen-bond inter-actions, with the formation of mol-ecular chains along the c axis.
Settore CHIM/08 - Chimica Farmaceutica
2008
Article (author)
File in questo prodotto:
File Dimensione Formato  
fj2107.pdf

accesso aperto

Tipologia: Publisher's version/PDF
Dimensione 735.76 kB
Formato Adobe PDF
735.76 kB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/54903
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 2
  • ???jsp.display-item.citation.isi??? 0
social impact