Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Iodoimidazo(1,2-a)pyridine | HCID 2764327 | — |
| Reactant | Hexabutyldistannane | HCID 6327815 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Imidazo(1,2-a)pyridine | HCID 78960 | — |
Reaction Steps
The obtained 2-[4′-(2″-hydroxyethoxy)]phenyl]-6-iodoimidazo[1,2-a]pyridine was dissolved in dioxane, and triethylamine is added thereto. Then, bis(tributyltin) and a catalytic amount of tetrakis-triphenylphosphine palladium are added thereto. This reaction mixture is heated at about 90° C. and reacted for about 24 hours, and then a solvent is distilled off and chromatographic purification is performed to obtain 6-tributylstannyl-2-[4′-(2″-hydroxyethoxy)]phenyl]imidazo[1,2-a]pyridine as the target compound (FIG. 2-2, Step 1). The amount of bis(tributyltin) to be used in this instance may be an amount satisfying a condition where it is excessive relative to the reaction substrate, specifically, it is about 1.5 times in molar ratio relative to the reaction substrate 2-[4′-(2″-hydroxyethoxy)phenyl]-6-iodoimidazo[1,2-a]pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08506930B2 |
|---|
| Source dataset | uspto-grants-2013_08 |
|---|
| ORD ID | ord-b63cc3ca6ea240f6a7ccd026ba0fb8f7 |
|---|
| Source note | uspto-grants-2013_08 |
|---|