Reaktion #11577

ord-327e302bf75244758d1922dd20b55bbb

Reaktionsgleichung

C1COCCO1.Cl
hydrogen chloride dioxane
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)[C@H]1CCCN1C(=O)OC(C)(C)C
(R)-1-(t-butoxycarbonyl)-2-pyrrolidinecarboxylic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)[C@H]1CCCN1.Cl
(R)-2-pyrrolidinecarboxylic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide hydrochloride

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooling
  2. 2
    EinengenThe reaction mixture was concentrated under reduced pressure

Vorschrift

Next, 4 N hydrogen chloride/dioxane (20 ml, 81 mmol) was added to (R)-1-(t-butoxycarbonyl)-2-pyrrolidinecarboxylic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide (1.8 g, 4.0 mmol) under ice-cooling, then the temperature was raised to room temperature, and the mixture was stirred for 1.5 hours. The reaction mixture was concentrated under reduced pressure to give 1.5 g (quantitatively) of (R)-2-pyrrolidinecarboxylic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide hydrochloride as a noncrystalline solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07098226B2uspto-grants-2006_08