HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 4-Bromo-1-hydroxyisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Bromo-1-chloro-7-isoquinolinesulphonyl chloride | HCID 18698401 | — |
| Reactant | HCID 178517620 | HCID 178517620 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Bromo-1-hydroxyisoquinoline | HCID 319772 | — |
Reaction Steps
4-Bromo-1-chloro-7-isoquinolinesulphonyl chloride ##STR198## A suspension of isoquinolinol (10 g, 68.9 mmol) in MeCN (250 ml) at 50° C., was treated with N-bromosuccinimide (12.6 g, 70.8 mmol) whereupon almost complete solution occurred before a thick white precipitate was formed. After heating under reflux for 3 h, the reaction mixture was cooled in ice and the solid filtered, washed with MeCN, and dried to afford 4-bromo-1-(2H)-isoquinolone (7.6 g, 34.0 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06093731 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-b0f146c8ff934f41aee8bfff8e9c916c |
| Source note | uspto-grants-2000_07 |