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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1500335Erstellt: 25. Oktober 2026

tert-Butyl methyl(3-oxopropyl)carbamate → Tert-butyl 3-(4-(dimethylamino)-4-phenylpiperidin-1-yl)propyl(methyl)carbamate

https://huagongshe.com/reaction/1500335

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl methyl(3-oxopropyl)carbamateHCID 10442454—
EduktN,N-dimethyl-4-phenylpiperidin-4-amine dihydrochlorideHCID 67366566—
EduktCID 101953985HCID 101953985—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
LösungsmittelChloroform methanolHCID 21584188—
ProduktTert-butyl 3-(4-(dimethylamino)-4-phenylpiperidin-1-yl)propyl(methyl)carbamateHCID 68494485—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

11.1 g (1.3 eq) tert-butyl methyl(3-oxopropyl)carbamate were added to a solution of 11 g (1 eq) N,N-dimethyl-4-phenylpiperidin-4-amine dihydrochloride in 110 ml methanol at 0° C. and the reaction mixture was stirred for 15 min at 0° C. 6.2 g (3 eq) sodium cyanoboron hydride were then added in portions and the mixture was stirred for 30 min at room temperature. The reaction mixture obtained was adjusted to a pH of 5-6 with acetic acid and stirred for 12 h at room temperature. The reaction course was monitored by thin-layer chromatography (20% MeOH/CHCl3). As the conversion was still not complete, 2.4 g sodium cyanoboron hydride were added and the reaction mixture obtained was adjusted to pH 5-6 with acetic acid and stirred for 60 min at room temperature.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09206156B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-f48332a52b454c169cd377fc55151a00
Quellennotizuspto-grants-2015_12