HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989853Generated: October 31, 2026
Sodium Chloride → 7-(Thiazol-4-yl)-2-(tri-n-butylstannyl)imidazo[5,1-b]thiazole
https://huagongshe.com/reaction/989853
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | 7-(Thiazol-4-yl)imidazo[5,1-b]thiazole | HCID 23449111 | — |
| Reactant | LiHMDS tetrahydrofuran | HCID 23714775 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-(Thiazol-4-yl)-2-(tri-n-butylstannyl)imidazo[5,1-b]thiazole | HCID 23449257 | — |
Reaction Steps
A solution of 1.01 g of 7-(thiazol-4-yl)imidazo[5,1-b]thiazole in 45 ml of THF was cooled to −70° C. in an argon atmosphere. Tri-n-butylstannyl chloride (1.58 ml) was added thereto. A 1 N lithiumbis(trimethylsilyl)amide/THF solution (11.2 ml) was added dropwise at the same temperature. The mixture was stirred for 30 min. The temperature of the mixture was raised to −30° C. over a period of one hr. A saturated aqueous sodium chloride solution was added thereto, followed by extraction twice with ethyl acetate. The extract was dried over anhydrous magnesium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:1). The title compound (294 mg) was obtained from the fraction of Rf=0.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06458780B1 |
|---|
| Source dataset | uspto-grants-2002_10 |
|---|
| ORD ID | ord-74279f7575134af1ac1b68f1ab7a9ba9 |
|---|
| Source note | uspto-grants-2002_10 |
|---|