HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromoisoquinoline → Isoquinoline, 5-bromo-, 2-oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromoisoquinoline | HCID 736487 | — |
| Reactant | Magnesium 2-(dioxidan-2-ide-1-carbonyl)benzoate--water (1/1/6) | HCID 21894687 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Isoquinoline, 5-bromo-, 2-oxide | HCID 22665708 | — |
Reaction Steps
3.1 A suspension of 6.24 g (30.0 mmol) of 5-bromoisoquinoline and 17.5 g (30 mmol) of magnesium monoperoxyphthalate hexahydrate (85%) in 120 ml of 2-propanol is stirred at room temperature for 50 hours. The reaction mixture is evaporated in vacuo, and saturated sodium chloride solution, saturated sodium hydrogencarbonate solution and dichloromethane are added. The organic phase is separated off and washed a number of times with saturated sodium chloride solution. The organic phase is dried over sodium sulfate and evaporated. The residue is stirred with tert-butyl methyl ether, giving 5-bromoisoquinoline 2-oxide as colourless crystals; HPLC/MS: 1.51 min, [M+H] 224/226.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08981101B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-16498351d1074d418446eca756809d60 |
| Source note | uspto-grants-2015_03 |