HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → HCID 23320188, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Fumarate | HCID 5460307 | — |
| Reactant | HCID 13362832 | HCID 13362832 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 23320188 | HCID 23320188 | — |
Reaction Steps
To a solution of 1-(3-aminobenzyl)-4-benzhydrylpiperazine (1.43 g) in a mixture of pyridine (3.2 g) and chloroform (20 ml) was dropwise added methanesulfonylchloride (0.31 ml) at 5° to 6° C. with stirring. The mixture was stirred at the same temperature for 30 minutes and at ambient temperature for 2 hours. The reaction mixture was concentrated and the resultant was extracted with ethyl acetate. The extract was washed with water, dried and evaporated in vacuo to give a residue. According to a conventional manner, the residue was converted to fumarate, which was recrystallized from ethanol to afford 1-(3-methanesulfonylaminobenzyl)-4-benzhydrylpiperazine fumarate (0.65 g) as yellow crystals. mp: 213°-215° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04591590 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-892c9eac1a6845d1a821c8e27435dd6d |
| Source note | uspto-grants-1986_05 |