Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 22345169 | HCID 22345169 | — |
| Product | Hydrogen Bromide | HCID 260 | — |
| Product | 2-Methanesulfonyl-4-(4-propyl-piperazin-1-yl)-phenol | HCID 22345218 | — |
Reaction Steps
1-(3-Methanesulfonyl-4-methoxy-phenyl)-4-propyl-piperazine (30 mg) was dissolved in 48-% HBr (2 ml) and stirred at 120° C. under an Argon-atmosphere for 3 h. The excess of HBr was then evaporated and absolute ethanol added and evaporated. This procedure was repeated several times to yield an residue of 2-Methanesulfonyl-4-(4-propyl-piperazin-1-yl)-phenol×HBr. MS m/z (relative intensity, 70 eV) 298 (M+, 35), 269 (bp), 226 (15), 199 (12), 70 (62).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06924374B2 |
|---|
| Source dataset | uspto-grants-2005_08 |
|---|
| ORD ID | ord-b8aeae07d70a44789d015e0ae6dd869c |
|---|
| Source note | uspto-grants-2005_08 |
|---|