HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Benzenesulfonyl)-5-bromo-1H-indole → 1-Benzenesulfonyl-5-[4-(4-benzyl-piperidin-1-yl)-but-1-ynyl]-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Benzenesulfonyl)-5-bromo-1H-indole | HCID 2776210 | — |
| Reactant | 1-(3-Butynyl)-4-benzylpiperidine | HCID 10609355 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Pyrrolidine | HCID 31268 | — |
| Product | 1-Benzenesulfonyl-5-[4-(4-benzyl-piperidin-1-yl)-but-1-ynyl]-1H-indole | HCID 18427956 | 80.3% |
Reaction Steps
A mixture of 1-benzenesulfonyl-5-bromoindole (1.34 g, 4 mmol), 4-benzyl-1-(3-butynyl)-piperidine (908 mg, 4 mmol) and tetrakis(triphenylphosphine)palladium (0) (600 mg) is stirred in pyrrolidine (50 mL) at 50° C. under N2 overnight. Most of the pyrrolidine is evaporated and the residue purified by medium-pressure column chromatography on silica gel eluting with 50% increasing to 100% EtOAc/hexanes to give the title compound as a pale yellow oil (1.55 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06448270B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-7997806fe34f44889798bd0d3a89202b |
| Source note | uspto-grants-2002_09 |