HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130436Generated: October 26, 2026
p-Bromobenzenesulfonyl chloride → 4-Bromo-N-[3-(cis-3,5-dimethyl-1-piperazinyl)-4-(methyloxy)phenyl]benzenesulfonamide
https://huagongshe.com/reaction/130436
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Bromobenzenesulfonyl chloride | HCID 7396 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 3-(cis-3,5-Dimethyl-1-piperazinyl)-4-(methyloxy)aniline | HCID 59007045 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Bromo-N-[3-(cis-3,5-dimethyl-1-piperazinyl)-4-(methyloxy)phenyl]benzenesulfonamide | HCID 11561539 | — |
Reaction Steps
A solution of 3-(cis-3,5-dimethyl-1-piperazinyl)-4-(methyloxy)aniline (D2) (800 mg, 3.40 mmol) in dichloromethane (50 ml) was treated with morpholinomethyl-polystyrene HL resin (1.70 g, 4.0 mmol/g loading, 6.80 mmol) followed by 4-bromobenzenesulfonyl chloride (1.30 g, 5.09 mmol). The resulting solution was stirred at room temperature overnight and was then filtered, washing with methanol, and the filtrate concentrated in vacuo. The residue was then purified using an SCX ion exchange cartridge (Varian bond-elute) eluting with methanol followed by ammonia (2M in methanol). The appropriate fractions were combined and reduced in vacuo to afford a crude product which was purified further by chromatography on silica gel eluting with (0 to 20% methanol in dichloromethane) to afford the title compound (E101). MS (ES+) m/e 454/456 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07381728B2 |
|---|
| Source dataset | uspto-grants-2008_06 |
|---|
| ORD ID | ord-a70442fd2070411aba07a4f6d225a94b |
|---|
| Source note | uspto-grants-2008_06 |
|---|