HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dimethyl-2-imidazolidinone → 2-Chloro-6-nitro-4-pentylaminoquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dimethyl-2-imidazolidinone | HCID 6661 | — |
| Reactant | Propylamine | HCID 7852 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 6-Nitro-2,4(1H,3H)-quinazolinedione | HCID 816982 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Chloro-6-nitro-4-pentylaminoquinazoline | HCID 18326391 | 70.1% |
Reaction Steps
To 400 mg (1.93 mmol) of 6-nitroquinazoline-2,4 (1H,3H)-dione were added 1 ml of 1,3-dimethyl-2-imidazolidinone and 6.58 g (42.91 mmol) of phosphorus oxychloride, and the resulting mixture was subjected to heating under reflux for 3 hours. After phosphorus oxychloride was removed in vacuo, the mixture was dissolved in 4 ml of acetonitrile, followed by addition of 5.60 ml (48.25 mmol) of propylamine and stirring under ice cooling for 30 minutes. To the reaction solution was added water, followed by extraction with ethyl acetate, washing with brine and drying over anhydrous sodium sulfate. After the solvent was distilled off, the residue was purified by a silica gel column to give 342 mg (yield: 70.1%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06339089B2 |
| Source dataset | uspto-grants-2002_01 |
| ORD ID | ord-0462c276a4144fca94d466f1c3282fd4 |
| Source note | uspto-grants-2002_01 |