HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 5-bromo-6-methoxyisoquinoline-N-oxide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 5-Bromo-6-methoxy-isoquinoline | HCID 22226545 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-bromo-6-methoxyisoquinoline-N-oxide hydrochloride | HCID 68878024 | 83.3% |
Reaction Steps
m-Chloroperbenzoic acid (1.4 g, 75%) was added in portions to a stirred solution of 5-bromo-6-methoxyisoquinoline (12 g, 5.04 mmol) in dichloromethane (12 ml). The mixture was stirred for 1 h then further dichloromethane (10 ml) added and the mixture stirred for an additional 2 h. Methanol (12 ml) was added and the mixture concentrated in vacuo to ˜9 ml, then 1M hydrochloric acid in diethyl ether (10 ml) was added. The mixture was diluted with ether and filtered, the precipitated solid was washed with diethyl ether and dried in vacuo to give crude 5-bromo-6-methoxyisoquinoline-N-oxide hydrochloride (1.22 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07618985B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-a3cddaab01a94e84accae8268c62de9f |
| Source note | uspto-grants-2009_11 |