HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → 8-(Benzyloxy)-3-iodoimidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 8-(Benzyloxy)imidazo[1,2-a]pyridine | HCID 13432974 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 8-(Benzyloxy)-3-iodoimidazo[1,2-a]pyridine | HCID 57355243 | — |
Reaction Steps
As shown in FIG. 6, N-iodosuccinimide (7.0 g, 31.2 mmol) was added to a solution of 8-benzyloxy-imidazo[1,2-α]pyridine (Example 19) 24 (7.0 g, 31.2 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 filtered and the cake washed with acetonitrile and water and dried under high vacuum to afford 8-benzyloxy-3-iodo-imidazo[1,2-α]pyridine 31 as colorless solid. 9.0 g, 83%, yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08618079B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-84648b43d76f481d941e1350468789d4 |
| Source note | uspto-grants-2013_12 |