HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984068Generated: October 29, 2026
Phosphorus pentachloride → 5-Chloro-2-(4-methyl-1-piperazinyl)benzoxazole
https://huagongshe.com/reaction/984068
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 178527795 | HCID 178527795 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 5-Chloro-2-(4-methyl-1-piperazinyl)benzoxazole | HCID 10848378 | — |
Reaction Steps
A 300 mg portion of 5-chloro-2-mercaptobenzoxazole was suspended in 50 ml of anhydrous benzene, and the suspension was mixed with 404 mg of phosphorus pentachloride and heated under reflux for 3 hours. The reaction solution was cooled in an ice bath and, with stirring, 1.6 g of 1-methylpiperazine was added thereto. After 30 minutes of stirring, the ice bath was removed to carry out 12 hours of stirring at room temperature, and then the reaction solution was mixed with saturated sodium bicarbonate aqueous solution and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried with magnesium sulfate and then the solvent was evaporated under a reduced pressure. Thereafter, the thus obtained mixture was purified by a silica gel column chromatography (ethyl acetate:methanol=20:1) to obtain the title compound (121 mg) in light yellow color.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06867226B2 |
|---|
| Source dataset | uspto-grants-2005_03 |
|---|
| ORD ID | ord-0972a410deb348e0969ea84742def335 |
|---|
| Source note | uspto-grants-2005_03 |
|---|