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HRID 51270Erstellt: 24. Oktober 2026

Veratrole → N-Boc-(2,3-dimethoxyphenyl)-4-piperidinylmethanone

https://huagongshe.com/de/reaction/51270

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktVeratroleHCID 7043—
Edukt4-(Methoxymethylcarbamoyl)piperidine-1-carboxylic acid tert-butyl esterHCID 44203202—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
ProduktN-Boc-(2,3-dimethoxyphenyl)-4-piperidinylmethanoneHCID 46780868—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of n-BuLi (2.5M, 452 mL) in hexane was added to a solution of veratrole (149 g, 1.08 mol) in anhydrous tetrahydrofuran (1.2 L) over 10 minutes at −78° C. under nitrogen. The resulting solution was stirred at 0° C. for 1 hour and room temperature for 4 hours. A solution of 4-[(methoxymethylamino)carbonyl]-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester (15) (275 g, 1.01 mol) in tetrahydrofuran (800 mL) was added to the reaction slurry at −65° C. over 20 minutes. The mixture was warmed to room temperature, stirred for 18 hours and quenched with saturated ammonium chloride (1 L). After stirring for 1 hour, the phases were separated and the aqueous layer was extracted with ethyl ether (1 L). The combined organic solutions were washed with brine (2 L) and dried (MgSO4). The mixture was filtered and the filtrate was concentrated (30° C./20 torr) to a residue (413 g). The solution may be used directly in Scheme L, step a, Example 108.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713627B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-74e44df03d06443bac63a75ca0bbbe91
Quellennotizuspto-grants-2004_03