HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 1-[(5-Chloroisoindol-2-yl)sulfonyl]piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | 1-Benzyl-4-[(5-chloroisoindol-2-yl)sulfonyl]piperazine | HCID 22710162 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 1-[(5-Chloroisoindol-2-yl)sulfonyl]piperazine | HCID 22709506 | — |
Reaction Steps
To a solution of 1-benzyl-4-[(5-chloroisoindol-2-yl)sulfonyl]piperazine (222 mg) in 1,2-dichloroethane (20 ml), 1-chloroethyl chloroformate (81 mg) was added under ice cooling. The resulting mixture was stirred for 15 minutes and then heated under reflux for 1 hour. After cooling, anhydrous methanol was added to the residue obtained by distilling off the solvent under reduced pressure. The mixture was heated under reflux for 11 hours. After cooling, the residue obtained by distilling off the solvent under reduced pressure was purified by chromatography on a silica gel column (ethanol:dichloromethane=1:50 to 1:10), whereby the title compound (120 mg, 70%) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06747023B1 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-f8520d48894a40f2a0e2d7c70c27bcaf |
| Source note | uspto-grants-2004_06 |