HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 7-(t-Butyldimethylsilylsulfamoyl)imidazo[5,1-b]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 7-Sulfamoylimidazo[5,1-b]thiazole | HCID 23449139 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-(t-Butyldimethylsilylsulfamoyl)imidazo[5,1-b]thiazole | HCID 17811066 | 108.8% |
Reaction Steps
t-Butyldimethylsilyl chloride (0.30 g) and 0.33 ml of triethylamine were added to a solution of 0.20 g of 7-sulfamoylimidazo[5,1-b]thiazole in 5ml of DMF. The mixture was stirred at room temperature for one hr. Ethyl acetate was added to the reaction mixture, followed by washing with water and saturated brine in that order. The organic layer was dried over anhydrous magnesium sulfate. The solvent was removed by distillation. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:1) to give 0.34 g of 7-(t-butyldimethylsilylsulfamoyl)imidazo[5,1-b]thiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06458780B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-e9ccdbaa84dd4a24908599001879875e |
| Source note | uspto-grants-2002_10 |