HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → 3-Iodo-imidazo[1,2-a]pyridine-8-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | Imidazo[1,2-a]pyridine-8-carbonitrile | HCID 15098893 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Iodo-imidazo[1,2-a]pyridine-8-carbonitrile | HCID 71757264 | 80% |
Reaction Steps
To a stirred solution of imidazo[1,2-a]pyridine-8-carbonitrile (1.2 g, 8.38 mmol) in dichloromethane (10 mL) was added N-iodosuccinimide (1.89 g, 8.38 mmol). LCMS monitored the reaction until the starting material consumed completely. The reaction mixture was diluted with dichloromethane and water. The separated organic layer was dried sodium sulfate, filtered and concentrated to give 3-iodoimidazo[1,2-a]pyridine-8-carbonitrile (1.8 g, 6.69 mmol, 80% yield) as a brown solid. MS (ES+) C8H81N3 requires: 269. found: 270 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08802697B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-1be97dbdfdfc4a988eb3b3be2dac7368 |
| Source note | uspto-grants-2014_08 |