Reaktion #161065

ord-5a20f2b4b1f940e0bcf30ae6f84b7d54

Reaktionsgleichung

O=C1C(=O)C2(CCCCC2)N=C1c1ccc[nH]1
2-(1H-pyrrol-2-yl)-3-oxo-1-azaspiro[4.5]dec-1-en-4-one
CC(C)[C@H](N)CO
L-valinol
CCOC(C)=O
ethyl acetate
CC(C)[C@@H](CO)NC(=O)C1(NC(=O)c2ccc[nH]2)CCCCC1
title compound
Ausbeute 76.4%
CC(C)[C@@H](CO)NC(=O)C1(NC(=O)c2ccc[nH]2)CCCCC1
N-[[1-[[(1H-Pyrrol-2-yl)carbonyl]amino]cyclohexyl]carbonyl]-L-valinol
Ausbeute 76.4%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.DISTILLATIONThe reaction solution was distilled off under reduced pressure
  2. 2
    Sonstigethe residue was purified by silica gel chromatography

Vorschrift

220 mg (1.01 mmol) of 2-(1H-pyrrol-2-yl)-3-oxo-1-azaspiro[4.5]dec-1-en-4-one was added to a solution of 252 mg (2.45 mmol) of L-valinol in 5 ml of ethyl acetate, and the mixture was stirred at room temperature for 4 days. The reaction solution was distilled off under reduced pressure and the residue was purified by silica gel chromatography to obtain 247 mg (76.4%) of the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08829209B2uspto-grants-2014_09