HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluoro-4-iodoaniline → HCID 18428007, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluoro-4-iodoaniline | HCID 185694 | — |
| Reactant | 4-(4-Chlorobenzyl)-1-(3-butynyl)piperidine | HCID 10682872 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Butylamine | HCID 8007 | — |
| Product | HCID 18428007 | HCID 18428007 | 18% |
Reaction Steps
To a solution of 4-(4-chlorobenzyl)-1-(but-3-yn-1-yl)piperidine (400 mg, 1.53 mmol) and 2-fluoro-4-iodoaniline (436 mg, 1.84 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 (100 mg, 18%): 1H NMR (CDCl3) 1.25 (m, 2 H), 1.46 (m, 1 H), 1.58 (m, 2 H), 1.97 (m, 2 H), 2.56 (m, 6 H), 2.88 (m, 2 H), 3.83 (bs, 2 H), 6.62 (m, 1 H), 6.80-7.24 (m, 6 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06130234 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-7625bb19436049009618a8740d7c3a3c |
| Source note | uspto-grants-2000_10 |