HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 7-Chloroacetylimidazo[5,1-b]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Imidazo[5,1-b]thiazole | HCID 21262404 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 7-Chloroacetylimidazo[5,1-b]thiazole | HCID 23449333 | — |
Reaction Steps
Chloroacetyl chloride (5.97 ml) was added to a solution of 12.5 g of aluminum chloride in 40 ml of 1,2-dichloroethane. The mixture was stirred at room temperature for 20 min. A solution of 1.93 g of imidazo[5,1-b]thiazole in 20 ml of 1,2-dichloroethane was added thereto. The mixture was heated under reflux for 2 hr. Water was added thereto, followed by extraction with dichloromethane. The organic layers were combined together. The combined organic layers were washed with a dilute aqueous sodium hydroxide solution and saturated brine in that order. The solvent was removed by distillation. Isopropyl ether was added to the residue. The resultant powder was collected by filtration to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06677331B2 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-4f5d5f2db3fb4a84878cf71c7032a9d8 |
| Source note | uspto-grants-2004_01 |