Reaktion #161064

ord-358193cf8fc1441086b9a39956151f40

Reaktionsgleichung

COc1ccc(C2=NC3(CCCCC3)C(=O)C2=O)cc1
2-(4-methoxyphenyl)-3-oxo-1-azaspiro[4.5]dec-1-en-4-one
CC(C)[C@H](N)CO
L-valinol
CCOC(C)=O
ethyl acetate
COc1ccc(C(=O)NC2(C(=O)N[C@H](CO)C(C)C)CCCCC2)cc1
title compound
Ausbeute 66.7%
COc1ccc(C(=O)NC2(C(=O)N[C@H](CO)C(C)C)CCCCC2)cc1
N-[[1-[[(4-Methoxyphenyl)carbonyl]amino]cyclohexyl]carbonyl]-L-valinol
Ausbeute 66.7%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.DISTILLATIONThe reaction solution was distilled off under reduced pressure
  2. 2
    Waschenthe residue was washed with diethyl ether

Vorschrift

260 mg (1.00 mmol) of 2-(4-methoxyphenyl)-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 washed with diethyl ether to obtain 243.5 mg (66.7%) of the title compound.

Quelle

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