HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 6-chloro-3-iodo-7-methoxy-2-methylquinolin-4(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | 6-chloro-7-methoxy-2-methylquinolin-4(1H)-one | HCID 49781464 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-chloro-3-iodo-7-methoxy-2-methylquinolin-4(1H)-one | HCID 67016702 | 89% |
Reaction Steps
To a stirred solution of 6-chloro-7-methoxy-2-methylquinolin-4(1H)-one (6.43 g, 28.7 mmol) and n-butylamine (28 ml, 287 mmol) in dimethylformamide (57 ml) cooled by a room temperature water bath was added iodine (7.30 g, 28.7 mmol) in a saturated solution of aqueous potassium iodide (29 ml). The reaction mixture was stirred 12 hours at room temperature. Residual iodine was quenched with 0.1 M aqueous sodium thiosulfate, and the resulting solution was concentrated in vacuo. The residue was resuspended in water and filtered to give 8.93 g (89% yield) of 6-chloro-3-iodo-7-methoxy-2-methylquinolin-4(1H)-one as a light brown powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598354B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-02c63bc650d64ef1a6497d9fb85a30e3 |
| Source note | uspto-grants-2013_12 |