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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77833Erstellt: 24. Oktober 2026

Trimethylsilylacetylene → 2,6-Pyridinediamine, 3-[2-(trimethylsilyl)ethynyl]-

https://huagongshe.com/de/reaction/77833

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylsilylacetyleneHCID 66111—
Edukt3-Iodopyridine-2,6-diamineHCID 476218—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt2,6-Pyridinediamine, 3-[2-(trimethylsilyl)ethynyl]-HCID 5925547160%

Reaktionsschritte

To a mixture of 3-iodo-pyridin-2,6-diamine (20.0 g, 85.2 mmol) described in Manufacturing Example 13-1-1, trimethylsilyl acetylene (24.2 mL, 170 mmol), copper (I) iodide (3.25 g, 17.0 mmol) N,N-diisopropylethylamine (19.1 g, 148 mmol) and N-methylpyrrolidinone (286 mL) was added tetrakis(triphenylphosphine)palladium (0) (9.81 g, 8.52 mmol) under argon atmosphere, which was stirred for 30 minutes at room temperature. The reaction solution was partitioned into water and ethyl acetate. The ethyl acetate layer was washed with water 4 times and dried over sodium sulfate, and the solvent was evaporated under a reduced pressure. The residue was purified by NH silica gel chromatography (heptane:ethyl acetate=4:1 then 1:1). The solids obtained by concentrating the eluate under a reduced pressure were washed with heptane containing a small amount of ethyl acetate to obtain the title compound (10.5 g, 60.0%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841327B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-8b516c37d4ea4c2baa72aa8bf98345ef
Quellennotizuspto-grants-2014_09