HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 7-(2-Methoxycarbonylvinyl)-2-(tri-n-butylstannyl)imidazo[5,1-b]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | LiHMDS tetrahydrofuran | HCID 23714775 | — |
| Reactant | 7-(2-Methoxycarbonylvinyl)imidazo[5,1-b]thiazole | HCID 69930338 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-(2-Methoxycarbonylvinyl)-2-(tri-n-butylstannyl)imidazo[5,1-b]thiazole | HCID 69927972 | — |
Reaction Steps
Tri-n-butylstannyl chloride (250 μl) and 2.1 ml of a 1.0 N lithiumbis(trimethylsilyl)amide/THF solution were added in that order to a solution of 7-(2-methoxycarbonylvinyl)imidazo[5,1-b]thiazole (a mixture of geometrical isomers) in dry THF in an argon atmosphere at −78° C. The mixture was stirred at the same temperature for 15 min. Water was added thereto. The mixture was extracted with ethyl acetate, followed by washing with saturated brine. The extract was dried over anhydrous magnesium sulfate and then filtered. The solvent was removed by distillation under the reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=4:1) to give 408 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06458780B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-fc55ba0d4c3f486cbc808b91634b0e30 |
| Source note | uspto-grants-2002_10 |