HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 1-(m-nitrophenyl)-3-methylquinazoline-2,4(1H, 3H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Dimethyl sulfite | HCID 69223 | — |
| Reactant | 1-(m-nitrophenyl)quinazoline-2,4(1H, 3H)-dione | HCID 12812377 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(m-nitrophenyl)-3-methylquinazoline-2,4(1H, 3H)-dione | HCID 12812378 | — |
Reaction Steps
To a solution of 2.8 g of 1-(m-nitrophenyl)quinazoline-2,4(1H, 3H)-dione and 30 ml of dimethylformamide was added 0.6 g of approximately 55 % sodium hydride, and the solution was stirred for 20 minutes at room temperature. To this was added 2.2 g of dimethyl sulfite and stirring was further continued for 4 hours at room temperature. After the reaction was complete, the solvent was removed from the reaction mixture by distillation under reduced pressure. The residue thus obtained was mixed with water to precipitate a crude product. This product was recrystallized from methanol to afford 2.8 g of 1-(m-nitrophenyl)-3-methylquinazoline-2,4(1H, 3H)-dione as colorless needles, melting at 242°-243° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04016166 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-0c4cbc72e24d4188a445601834301607 |
| Source note | uspto-grants-1977_04 |