HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-[4-(2,4-Dichlorobenzoyl)benzyl]thio-3-methyl-4(3H)-quinazolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(2,4-Dichlorobenzoyl)benzyl bromide | HCID 18919279 | — |
| Reactant | HCID 178481666 | HCID 178481666 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[4-(2,4-Dichlorobenzoyl)benzyl]thio-3-methyl-4(3H)-quinazolinone | HCID 18919337 | 91.2% |
Reaction Steps
To a solution of 2-mercapto-3-methyl-4(3H)-quinazolinone (1.0 g) and sodium hydroxide (250 mg) in 50% ethanol (15 ml)-DMF (15 ml) was added 4-(2,4-dichlorobenzoyl)benzyl bromide (1.88 g) and the mixture was stirred at room temperature for 1 hour. This reaction mixtrue was poured in water and the resulting crystals were collected by filtration, rinsed with water and methanol, and recrystallized from methanol to provide the title compound as colorless solid (2.16 g). IH-NMR (CDCl3) δ: 3.59(3H,s), 4.59(2H,s), 7.25-7.80(10H,m), 8.22(1H,dd,J=8.2,1.4Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753664 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-970672ce441a42019c7b678f497f586b |
| Source note | uspto-grants-1998_05 |