HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 7-fluoro-1-methyl-3-(1-methyl-1H-tetrazol-5-yl)-4-quinolone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1-(4-fluoro-2-methylaminophenyl)-2-(1-methyl-1H-tetrazol-5-yl)ethanone | HCID 13474394 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 7-fluoro-1-methyl-3-(1-methyl-1H-tetrazol-5-yl)-4-quinolone | HCID 13474453 | — |
Reaction Steps
A mixture of acetic anhydride (0.8 ml) and formic acid (0.4 ml) was stirred at 50°-60° for 2 hours, then cooled to ambient temperature. 1-(4-Fluoro-2-methylaminophenyl)-2-(1-methyl-1H-tetrazol-5-yl)ethanone (1.03 g) was added. The mixture was stirred at ambient temperature for 5 hours, then kept at this temperature for 16 hours. The mixture was triturated under light petroleum to give a solid product. This product was extracted with boiling ethyl acetate (100 ml) and the extract cooled to give a solid product which was recrystallised from industrial methylated spirit to give the novel compound 7-fluoro-1-methyl-3-(1-methyl-1H-tetrazol-5-yl)-4-quinolone, m.p. 264°-267°, identical to the product of Example 2(d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04659718 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-2643c1bc739042ee89fffc15a694f755 |
| Source note | uspto-grants-1987_04 |