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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 10409Erstellt: 23. Oktober 2026

Diisopropylamine → 4-Bromo-2-[4-(2-(R)-methyl-pyrrolidin-1-yl)-but-1-ynyl]-phenylamine

https://huagongshe.com/de/reaction/10409

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
Edukt4-Bromo-2-iodoanilineHCID 823934—
Edukt(R)-1-(But-3-yn-1-yl)-2-methylpyrrolidineHCID 11367023—
Edukt1-Butyn-3-yl-2-methyl-pyrrolidineHCID 21980062—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Katalysator5-Bromo-2-benzothiazoleethanolHCID 21980060—
Produkt4-Bromo-2-[4-(2-(R)-methyl-pyrrolidin-1-yl)-but-1-ynyl]-phenylamineHCID 2104149497,3%

Reaktionsschritte

To a solution of 1-butyn-3-yl-2-methyl-pyrrolidine in CH3CN (prepared in Example 65A assuming 100% conversion, 89 mmol) was added 4-bromo-2-iodo-phenylamine (12.0 g, 40 mmol) under nitrogen followed by addition of CuI (0.38 g, 2.0 mmol), PdCl2(PPh3) 2 (0.70 mg, 1.0 mmol) and diisopropylamine (33.6 mL, 240 mmol). The resulting solution was stirred at room temperature for 2 hours, at which time analytical HPLC analysis indicated that all 4-bromo-2-iodo-phenylamine was consumed. The solvent CH3CN was removed under vacuo and the residue was extracted with IPAC (500 mL) and 5% NaHCO3 (2×300 mL). The organic layer was washed with brine, dried over Na2SO4 and concentrated under reduced pressure to give the title compound as a thick oil (11.96 g), which was used in the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07094790B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-3e0d8478526940bf83b3ecdefee834a4
Quellennotizuspto-grants-2006_08