HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 1-(3-bromopropyl)-3-methyl-2,4(1H)-quinazolinedione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(3-bromopropyl)-2,4(1H,3H)-quinazolinedione | HCID 13687207 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(3-bromopropyl)-3-methyl-2,4(1H)-quinazolinedione | HCID 13687208 | 62.3% |
Reaction Steps
A mixture of 1-(3-bromopropyl)-2,4(1H,3H)-quinazolinedione (2.83 g), methyl iodide (3 ml), anhydrous potassium carbonate (4.2 g) and N,N-dimethylformamide (25 ml) was stirred for 8 hours at ambient temperature. After the reaction mixture was diluted with cold water, the resultant mixture was extracted twice with chloroform. The chloroform layer was washed with water twice, and with saturated sodium chloride aqueous solution, dried over anhydrous magnesium sulfate and evaporated in vacuo. The resultant oily residue was purified by subjecting to a column chromatography on silica gel (100 g) using chloroform for elution, to give 1-(3-bromopropyl)-3-methyl-2,4(1H,3H)-quinazolinedione (1.85 g) as a crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04608375 |
| Source dataset | uspto-grants-1986_08 |
| ORD ID | ord-533da7f8d4e34289b10d5d5aa6b3a3f9 |
| Source note | uspto-grants-1986_08 |