HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Amino-2-methylphenol → HCID 22478272, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Amino-2-methylphenol | HCID 17818 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 135513647 | HCID 135513647 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 22478272 | HCID 22478272 | 81% |
Reaction Steps
A mixture of 6,7-dimethoxy-5-nitro-3,4-dihydroquinazolin-4-one (1.75 g, 7.0 mmol) and thionyl chloride (25 ml) and DMF (3 drops) was heated at reflux for 2 hours. Excess thionyl chloride was removed by evaporation and the residue azeotroped with toluene. 3-Hydroxy-4-methylaniline (0.94 g, 7.6 mmol) in 2-propanol (40 ml) was added to the residue and the mixture heated at reflux for 2 hours. The mixture was allowed to cool, the precipitate collected by filtration, washed with 2-propanol and dried to give 6,7-dimethoxy-4-(3-hydroxy-4-methylanilino)-5-nitroquinazoline hydrochloride (2.02 g, 81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE042353E1 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-ea67b57407444abd995e8b20ff64996d |
| Source note | uspto-grants-2011_05 |