HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → 5-Iodo-2-methyl-1,7-naphthyridin-8(7H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | HCID 22090499 | HCID 22090499 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Iodo-2-methyl-1,7-naphthyridin-8(7H)-one | HCID 68620721 | 80.1% |
Reaction Steps
2-Methyl-7H-[1,7]naphthyridin-8-one (10.0 g, 62.4 mmol) was suspended in 300 ml acetonitrile and N-iodosuccinimide (16.9 g, 74.9 mmol) was added. The suspension was stirred for 3 hours at reflux. The reaction mixture was cooled to room temperature and filtered. The solid was washed with acetonitrile and dried for 30 minutes at 50° C. and <20 mbar, to get the desired compound as a brown solid (14.3 g, 80%), MS: m/e=287.0 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07511055B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-6b8d0b48d52746f0ac11612a6701e8e3 |
| Source note | uspto-grants-2009_03 |