HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 4-(4-Benzylpiperazin-1-yl)-1-(phenylsulfonyl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(Phenylsulfonyl)-4-(1-piperazinyl)-1h-indole | HCID 10154392 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(4-Benzylpiperazin-1-yl)-1-(phenylsulfonyl)-1H-indole | HCID 10274390 | — |
Reaction Steps
A solution of 1-(phenylsulfonyl)-4-piperazin-1-yl-1H-indole (71 mg, 0.18 mmol) in tetrahydrofuran is treated sequentially with benzyl bromide (21 μl) and triethyl-amine (75 μl), shaken at room temperature for 16 hr and concentrated in vacuo to give a residue. The residue is purified by RP-HPLC to give the title product, 37 mg, identfied by HPLC and mass spectral analyses (2.81 min; 432 M+H) using the LCMS conditions described in Table I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07034029B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-dde47df13b184e5f915c8f1eab188257 |
| Source note | uspto-grants-2006_04 |