HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-Amino-6-chloro-4-phenyl-3,4-dihydroquinazolin-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 5-Chloro-2-(((dimethylamino)methylene)amino)benzophenone | HCID 20360437 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Amino-6-chloro-4-phenyl-3,4-dihydroquinazolin-4-ol | HCID 119679 | 95% |
Reaction Steps
To a solution of 0.29 part of 5-chloro-2-dimethylaminomethyleneaminobenzophenone in 4 volume parts of ethanol are added 0.2 volume part of hydrazine hydrate and 0.06 volume part of glacial acetic acid. The mixture is shaken and kept standing at room temperature for about 30 minutes. The resulting crystals are recovered by filtration and washed with ethanol and then dried, whereby 3-amino-6-chloro-3,4-dihydro-4-hydroxy-4-phenylquinazoline is obtained as colorless needles melting at 185° (softening) to 192° C. This compound is identical with the product obtained in Example 1. Yield: 95%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04082764 |
| Source dataset | uspto-grants-1978_04 |
| ORD ID | ord-0d4feaeec8f64891a889f6fae85d059c |
| Source note | uspto-grants-1978_04 |