HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → 2-Ethyl-3-iodoimidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 2-Ethylimidazo[1,2-a]pyridine | HCID 21831991 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Ethyl-3-iodoimidazo[1,2-a]pyridine | HCID 130054803 | — |
Reaction Steps
As shown in FIG. 8, N-iodosuccinimide (8.37 g, 57.25 mmol) was added to a solution of 2-ethyl-imidazo[1,2-α]pyridine 70 (Example 27) (12.88 g, 57.25 mmol) in dry acetonitrile (100 mL) at 0° C. The reaction was warmed to room temperature and then stirred for 12 hours. The mixture was then concentrated and purified on silica gel (CombiFlash, Heptane/EtOAc elution) to afford 2-ethyl-3-iodo-imidazo[1,2-α]pyridine 72, as photosensitive yellow crystals with a yield of 5.6 g, 35%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08618079B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-577970f1637c4aceaadce2642be712d7 |
| Source note | uspto-grants-2013_12 |