HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(3-chlorophenyl)-4,5-dihydro-alpha-(4-methoxyphenyl)-alpha-(1-methyl-1H-imidazol-5-yl)-tetrazolo[1,5-a]quinazoline-7-methanol → 9-(3-chlorophenyl)-4,9-dihydro-alpha-(4-methoxyphenyl)-alpha-(1-methyl-1H-imidazol-5-yl)-tetrazolo[5,1-b]quinazoline-7-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(3-chlorophenyl)-4,5-dihydro-alpha-(4-methoxyphenyl)-alpha-(1-methyl-1H-imidazol-5-yl)-tetrazolo[1,5-a]quinazoline-7-methanol | HCID 136342082 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 9-(3-chlorophenyl)-4,9-dihydro-alpha-(4-methoxyphenyl)-alpha-(1-methyl-1H-imidazol-5-yl)-tetrazolo[5,1-b]quinazoline-7-methanol | HCID 136096424 | 27% |
Reaction Steps
A mixture of intermediate 17 (0.0006 mol) in toluene (10 ml) was stirred and refluxed for 5 hours, then brought to room temperature and the solvent, was evaporated till dryness. The residue was taken up in DCM. The solvent was evaporated till dryness. The residue was purified by column chromatography over kromasil® (10 μm) (eluent: DCM/MeOH/Et3N 95/5/0.5). The pure fractions were collected and the solvent was evaporated. The residue (0.12 g, 40%) was taken up in DCM. The solvent was evaporated till dryness, yielding 0.08 g (27%) of 9-(3-chlorophenyl)-4,9-dihydro-α-(4-methoxyphenyl)-α-(1-methyl-1H-imidazol-5-yl)-tetrazolo[5,1-b]quinazoline-7-methanol (compound 3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07511138B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-ee20223f472244bfac1603ceaa338f24 |
| Source note | uspto-grants-2009_03 |