3‐ tert ‐Butyl‐7,7‐di­methyl‐1‐phenyl‐5,6,7,8‐tetra­hydro­imidazo­[3,4‐ b ]­quinolin‐5‐one and 2,8,8‐tri­methyl‐5‐phenyl‐6,7,8,9‐tetrahydroimidazo­[2,3‐ a ]­quinolin‐6‐one: chains generated by C—H⋯N hydrogen bonds | Zendy

Low John N. | Zendy; Cobo Justo | Zendy; Mera Jaime | Zendy; Quiroga Jairo | Zendy; Glidewell Christopher | Zendy

Open Access

3‐ tert ‐Butyl‐7,7‐dimethyl‐1‐phenyl‐5,6,7,8‐tetrahydroimidazo[3,4‐ b ]quinolin‐5‐one and 2,8,8‐trimethyl‐5‐phenyl‐6,7,8,9‐tetrahydroimidazo[2,3‐ a ]quinolin‐6‐one: chains generated by C—H⋯N hydrogen bonds

Author(s) -

Low John N.,

Cobo Justo,

Mera Jaime,

Quiroga Jairo,

Glidewell Christopher

Publication year - 2004

Publication title -

acta crystallographica section c

Language(s) - English

Resource type - Journals

eISSN - 1600-5759

pISSN - 0108-2701

DOI - 10.1107/s0108270104011291

Subject(s) - naphthalene , molecule , chemistry , ring (chemistry) , delocalized electron , stereochemistry , medicinal chemistry , hydrogen bond , organic chemistry

In both 3‐ tert ‐butyl‐7,7‐dimethyl‐1‐phenyl‐5,6,7,8‐tetrahydroimidazo[3,4‐ b ]quinolin‐5‐one, C 22 H 25 N 3 O, (I), and 2,8,8‐trimethyl‐5‐phenyl‐6,7,8,9‐tetrahydroimidazo[2,3‐ a ]quinolin‐6‐one, C 19 H 19 N 3 O, (II), the heterobicyclic portions of the molecules are planar, with naphthalene‐type delocalization in (II), while the carbocyclic ring in each compound adopts an envelope conformation. In both (I) and (II), the molecules are linked weakly into chains by a single C—H⋯N hydrogen bond.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.

Having issues? You can contact us here

Accelerating Research