HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 7-(4-Nitrobenzylsulfamoyl)imidazo[5,1-b]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Nitrobenzylamine | HCID 29147 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 23449038 | HCID 23449038 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-(4-Nitrobenzylsulfamoyl)imidazo[5,1-b]thiazole | HCID 23449305 | 74.1% |
Reaction Steps
4-Nitrobenzylamine (1.24 g) and 2 ml of diisopropylethylamine were added to a solution of 0.95 g of 7-chlorosulfonylimidazo[5,1-b]thiazole in 20 ml of DMF. The mixture was stirred at room temperature for 12 hr. Ethyl acetate was added to the reaction mixture. The mixture was washed with water and saturated brine in that order. The organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated, and the resultant powder was collected by filtration to give 1.07 g of 7-(4-nitrobenzylsulfamoyl)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-b3b9a4c34b004c4388e24bbbf71fe742 |
| Source note | uspto-grants-2002_10 |