Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Pentyne, 5-chloro- | HCID 84308 | — |
| Reactant | 3-Iodobenzene-1,2-diamine | HCID 18510485 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Product | HCID 18510476 | HCID 18510476 | 92% |
Reaction Steps
To a stirred solution of 2-amino-3-iodoaniline (13 g) in triethylamine (260 ml) were added bis(triphenylphosphine) palladium dichloride (2 g) and copper (I) iodide (1.15 g). The mixture was cooled to 5° C. before the addition of 5-chloro-1-pentyne (6.6 ml). The mixture was heated to 50° C. and stirred 5 h. The mixture was cooled to room temperature, filtered and evaporated. The residue was purified by column chromatography on silica gel (ethyl acetate/hexane 1:1 to 5:1 eluant) to afford 3-(5-chloropent-1-ynyl)-pyridin-2-ylamine as a red oil (10.6 g, 92%): MS (EI) 196, 194 (M),159, 157, 131, 104; 1H NMR (δ, CDCl3) 8.0 (dd, 1H, J=2,5 Hz), 7.47 (dd, 1H, J=2,7 Hz), 6.59 (dd, 1H, J=5,7 Hz), 4.94 (br s, 1H), 3.72 (t,2H, J=6 Hz), 2.68 (t,2H, J=7 Hz), 2.07 (dt,2H, J=6,7 Hz) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06583134B2 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-80daac2a75c34f339aeffe3e097c17b7 |
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| Source note | uspto-grants-2003_06 |
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