HuagongsheHuagongshe Chemistry Print Report · For research reference only
8-Chlorotheophylline → 8-Chloro-7-[4-(4-chlorobenzoyl)benzyl]-1,3-dimethylxanthine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 8-Chlorotheophylline | HCID 10661 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(4-Chlorobenzoyl)benzyl bromide | HCID 9839651 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-Chloro-7-[4-(4-chlorobenzoyl)benzyl]-1,3-dimethylxanthine | HCID 18919038 | 75.2% |
Reaction Steps
To a solution of 8-chlorotheophylline (2.15 g) in DMF (20 ml) was added potassium carbonate (1.66 g) as well as 4-(4-chlorobenzoyl)benzyl bromide (3.10 g) and the mixture was stirred at room temperature for 20 hours. This reaction mixture was diluted with water and extracted with ethyl acetate. The extract was washed with saturated aqueous NaCl solution and dried over anhydrous sodium sulfate. The solvent was then distilled off and the residue was washed with ether to provide the title compound as white powder (3.34 g, 75%). 1H-NMR (CDCl3) 6: 3.41(3H,s), 3.57(3H,s), 5.64(2H,s), 7.41-7.52(4H,m), 7.68-7.80(4H,m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753664 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-8e792f3ac9674844898138fa6639107f |
| Source note | uspto-grants-1998_05 |