HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 10426535, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 10421619 | HCID 10421619 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10426535 | HCID 10426535 | — |
Reaction Steps
To a solution of 11-amino-4,5-dihydro-1H-pyrazolo[3,4-a]acridine (2.36 g) in dry DMF (90 ml) was added NaH (60%)(0.50 g) slowly. The reaction was stirred at room temperature for 15 minutes and then benzyl bromide (1.88 g) was added and the reaction was stirred an additional 15 minutes. At the end of this time the product was precipitated with water, filtered off, washed well with water, and air dried to yield a product which was further purified by flash chromatography (5% Et3N-EtOAc). The product-containing fractions were combined, concentrated, and recrystallized from EtOAc to give 2.35 g, mp 206°-207°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05179100 |
| Source dataset | uspto-grants-1993_01 |
| ORD ID | ord-93f7926f45384f12a64009d6c10eb067 |
| Source note | uspto-grants-1993_01 |