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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 60900Erstellt: 24. Oktober 2026

Carbamate → (2S,3R)-Allyl 2-(aminomethyl)-3-methylpiperidine-1-carboxylate

https://huagongshe.com/de/reaction/60900

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbamateHCID 276—
EduktAllyl chloroformateHCID 18052—
EduktHydrazine hydrate (1:1)HCID 24654—
EduktDiisopropylethylamineHCID 81531—
Edukt2-(((2S,3R)-3-Methylpiperidin-2-yl)methyl)isoindoline-1,3-dioneHCID 117727630—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
Produkt(2S,3R)-Allyl 2-(aminomethyl)-3-methylpiperidine-1-carboxylateHCID 89748216—

Reaktionsschritte

To a solution of 2-(((2S,3R)-3-methylpiperidin-2-yl)methyl)isoindoline-1,3-dione (5 g, 19.4 mmol) in CH2Cl2 at 0° C. was added DIPEA (3.8 mL), followed by allyl chloroformate (2.6 mL). The reaction was allowed to warm to rt overnight. After 16 h, the reaction was concentrated to remove the CH2Cl2, and then re-suspended in EtOAc and washed with 1 M HCl (2×), brine (2×), dried (MgSO4) and concentrated to give the crude carbamate which was used without further purification. A mixture of the crude carbamate and hydrazine hydrate (2 g, 39 mmol) in MeOH (100 mL) was heated at 60° C. for 2 h. The mixture was cooled to rt and the solvent was removed in vacuo. The crude was dissolved in EtOAc and washed with 2 N NaOH (2×), brine, and then dried (Na2SO4). The solvent was removed in vacuo to obtain the title compound which was used without further purification. ESI-MS (m/z): 213 [M+1]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09440982B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-fbf016bb74e441ada4a45e7d402b144f
Quellennotizuspto-grants-2016_09