## Abstract For Abstract see ChemInform Abstract in Full Text.
9-Methyl-2,6-di-p-tolyl-2,3,6,7-tetrahydro-1H,5H-pyrimido[5,6,1-ij]quinazoline
β Scribed by Mahon, Andrew B. ;Craig, Donald C. ;Try, Andrew C.
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 404 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
No coin nor oath required. For personal study only.
β¦ Synopsis
The title compound, C~25~H~27~N~3~, possesses an essentially planar, fused tricyclic platform, from which two p-tolyl rings project on the same face to create a hydrophobic pocket.
π SIMILAR VOLUMES
The title compound, C 23 H 25 BrO 3 , was synthesized by the reaction of p-bromobenzaldehyde with dimedone and HClO 4 / SiO 2 in EtOH. In the molecule, the dihydropyran ring adopts a boat conformation and the two cyclohexene rings are in a trans conformation.
In the title compound, C 12 H 18 O 5 , the ring has a chair conformation, with endocyclic torsion angle magnitudes in the range 47.7 (3)-66.7 (2) . The OH group donates an intermolecular hydrogen bond to a C O group with an OΓ Γ ΓO distance of 2.791 (3) A Λ, forming chains. organic papers o2662 Burt