HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ammonia → 3,4-Dimethoxy-6-nitrobenzamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ammonia | HCID 222 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | 4,5-Dimethoxy-2-nitrobenzoic acid | HCID 78690 | — |
| Produkt | 3,4-Dimethoxy-6-nitrobenzamide | HCID 2736193 | — |
Reaktionsschritte
4,5-Dimethoxy-2-nitrobenzoic acid (3) was treated with thionyl chloride and then reacted with ammonia to give 4,5-dimethoxy-2-nitrobenzamide (4) as described by F. Nomoto et al. Chem. Pharm. Bull., 1990, 38, 1591-1595. The nitro group in compound (4) was reduced with sodium borohydride in the presence of copper sulfate (see C.L. Thomas, Catalytic Processes and Proven Catalysts, Academic Press, New York (1970)) to give 4,5-dimethoxy-2-aminobenzamide (5) which was cyclized by refluxing with formic acid to give 6,7-dimethoxyquinazoline-4(3H)-one (6). Compound (6) was refluxed with phosphorus oxytrichloride to provide the common synthetic precursor (7).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06313130B1 |
| Quelldatensatz | uspto-grants-2001_11 |
| ORD ID | ord-8be6a258a91d45d784672c58bba29202 |
| Quellennotiz | uspto-grants-2001_11 |