Download citation
Download citation

link to html
The title compound, C31H44O5, was synthesized from isostev­iol (systematic name: ent-16-ketobeyeran-19-oic acid). In the mol­ecule, the three six-membered rings adopt chair conformations and the stereochemistry of the A/B and B/C ring junctions are trans. The five-membered ring D adopts an envelope conformation with the methyl­ene C atom as the flap.

Download citation
Download citation

link to html
The title compound, C32H28N6O4·2C2H5OH, consists of two 2-(propyl­amino)­benzofuro[3,2-d]pyrimidin-4(3H)-one units connected, via one of the pyrimidine N atoms, to a bridging benzene ring in the 1,4 positions. Two ethanol solvent mol­ecules are also present. The main mol­ecule lies on a center of symmetry located at the center of the benzene ring. The fused-ring system of the benzofuro[3,2-d]pyrimidine moiety is nearly planar (r.m.s. deviation = 0.016 Å) and forms a dihedral angle of 78.21 (7)° with the central benzene ring. The crystal structure features O—H...O and N—H...O inter­actions. The C atoms of the propyl­amino side chain in the main mol­ecule and the ethyl group in the solvent mol­ecule are disordered over two positions, with site-occupancy factors 0.34:0.66 and 0.42:0.58, respectively.

Download citation
Download citation

link to html
In the title compound, C30H41NO6, the three six-membered rings adopt chair conformations and the stereochemistry of the A/B and B/C ring junctions are trans. The five-membered ring D adopts an envelope conformation, with the methyl­ene C atom as the flap. The title compound was synthesized via esterification, Tollens reaction, 1,5-hydride shift from the natural tetracyclic diterpenoid isosteviol
Follow Acta Cryst. E
Sign up for e-alerts
Follow Acta Cryst. on Twitter
Follow us on facebook
Sign up for RSS feeds