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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16589Erstellt: 25. Oktober 2026

Diisopropylethylamine → Methyl 1-[(4-{[(tert-butoxycarbonyl)amino]methyl}piperidine-1-yl)methyl]cyclopentanecarboxylate

https://huagongshe.com/reaction/16589

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktTert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
EduktMethyl 1-(iodomethyl)cyclopentanecarboxylateHCID 67231596—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
LösungsmittelSodium BicarbonateHCID 516892—
ProduktMethyl 1-[(4-{[(tert-butoxycarbonyl)amino]methyl}piperidine-1-yl)methyl]cyclopentanecarboxylateHCID 6723246967,2%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

A mixture of Methyl 1-(iodomethyl)cyclopentanecarboxylate(5.52 g, 0.0206 mol, Step 1), tert-butyl(piperidin-4-ylmethyl)carbamate (8.83 g, 0.0412 mol) and iPr2NEt (10.76 mL, 0.0618 mol) in N-methylpyrrolidone (70 mL) was stirred at 120° C. for 24 h. After cooling, the reaction mixture was diluted with sat. NaHCO3 aq. (200 mL), extracted with AcOEt (200 mL) for three times, and the combined organic layer was washed with water (200 mL) and brine (200 mL). The organic layer was dried over Na2SO4, filtered and concentrated. Removal of the solvent gave a residue, which was chromatographed on a column of silica gel eluting with EtOAc/hexane (1:1) to give 4.91 g (67%) of title compound as a yellow syrup.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737163B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-7979378220074b7c996aa06eafdcf99f
Quellennotizuspto-grants-2010_06