HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
3-Methylbut-1-yne → 2-Chloro-5-(3-methylbut-1-ynyl)pyridin-4-amine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 3-Methylbut-1-yne | HCID 69019 | — |
| Edukt | 2-Chloro-5-iodopyridin-4-amine | HCID 45480366 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Katalysator | HCID 178418476 | HCID 178418476 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | 2-Chloro-5-(3-methylbut-1-ynyl)pyridin-4-amine | HCID 58025064 | — |
Reaktionsschritte
To a solution of 2-chloro-5-iodopyridin-4-amine (Compound 11, 2.55 g, 10.0 mmol) in Et3N (35 ml) was added Pd(PPh3)2Cl2 (70 mg, 0.10 mmol), CuI (19 mg, 0.10 mmol), and 3-methyl-1-butyne (1.2 ml, 12 mmol). The reaction was stirred at room temperature for 20 h and was quenched with H2O, extracted with EtOAc (Δ2). The combined organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by chromatography on silica gel (0→30% EtOAc-hexanes) to yield the title compound as an off-white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08536339B2 |
| Quelldatensatz | uspto-grants-2013_09 |
| ORD ID | ord-c536abf1d78f45489380ea426fc5482d |
| Quellennotiz | uspto-grants-2013_09 |