HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)- → 6-Amino-9-benzyl-8-hydroxy-2-(3-phthalimidopropylthio)purine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)- | HCID 11325 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Amino-9-benzyl-8-hydroxy-2-mercaptopurine | HCID 178509059 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Amino-9-benzyl-8-hydroxy-2-(3-phthalimidopropylthio)purine | HCID 178509045 | 75% |
Reaction Steps
6-Amino-9-benzyl-8-hydroxy-2-mercaptopurine (110 mg, 0.40 mmol) was suspended in dimethylformamide (10 ml). To the suspension were added potassium carbonate (50 mg, 0.40 mmol) and 2-phthalimidoethyl bromide (108 mg, 0.40 mmol) in order. The mixture was stirred at room temperature for 2 hours. The solvent was removed in vacuo, water and methanol were added to the residue, and the resulting crystals were taken by filtration to give the subject compound (138 mg, yield 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329381B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-5f1899c1cbe748bbb5bed8fd6977008e |
| Source note | uspto-grants-2001_12 |