HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Iodoaniline → 1-(4-(4-Aminophenyl)-3-butynyl)-4-(4-chlorobenzyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Iodoaniline | HCID 10893 | — |
| Reactant | 4-(4-Chlorobenzyl)-1-(3-butynyl)piperidine | HCID 10682872 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Butylamine | HCID 8007 | — |
| Product | 1-(4-(4-Aminophenyl)-3-butynyl)-4-(4-chlorobenzyl)piperidine | HCID 10618025 | 12% |
Reaction Steps
To a solution of 4-(4-chlorobenzyl)-1-(but-3-yn-1-yl)piperidine (318 mg, 1.21 mmol) and 4-iodoaniline (265 mg, 2.19 mmol) in 10 mL of butylamine is added 70 mg of Pd(PPh3)4. The resulting solution is allowed to reflux for 24 hr. The solvent is evaporated in vacuo and the residue is purified by flash chromatography giving the title product as a brown oil (50 mg, 12%): 1H NMR (CDCl3) 1.24 (m, 2 H), 1.44 (m, 1 H), 1.58 (m, 2 H), 1.96 ( m, 3 H), 2.15 (m, 2 H), 2.55 (m, 4 H), 2.89 (m, 2 H), 3.75 (bs, 2 H), 6.53 (d, J=6.0 Hz, 2 H), 7.05 (m, 2 H), 7.20 (m, 4 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06448270B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-53b0ceb41ec344188db13bb98c1b88a8 |
| Source note | uspto-grants-2002_09 |