N-Methylpiperidine → N1-[2-(4-cyanophenoxy)-1-methylethyl]-N2-(4-methylbenzyloxycarbonyl)-L-valinamide

HRID 1900176

Reaktionsgleichung

Reaktionsgleichung von HRID 1900176
CN1CCCCC1.[CH3:8][C:9]1[CH:26]=[CH:25][C:12]([CH2:13][O:14][C:15]([NH:17][C@H:18]([C:22]([OH:24])=O)[CH:19]([CH3:21])[CH3:20])=[O:16])=[CH:11][CH:10]=1.ClC(OCC(C)C)=O.[C:35]([C:37]1[CH:47]=[CH:46][C:40]([O:41][CH2:42][CH:43]([NH2:45])[CH3:44])=[CH:39][CH:38]=1)#[N:36]>C(Cl)Cl.O>[C:35]([C:37]1[CH:47]=[CH:46][C:40]([O:41][CH2:42][CH:43]([NH:45][C:22](=[O:24])[C@H:18]([CH:19]([CH3:20])[CH3:21])[NH:17][C:15]([O:14][CH2:13][C:12]2[CH:11]=[CH:10][C:9]([CH3:8])=[CH:26][CH:25]=2)=[O:16])[CH3:44])=[CH:39][CH:38]=1)#[N:36]

Komponenten

7

Edukt 4

HCID 12291N-MethylpiperidineHCID 62365Isobutyl chloroformateHCID 189727992-(4-Cyanophenoxy)-1-methylethylamineHCID 54315643N-(4-methylbenzyloxycarbonyl)-L-valine

Produkt 1

HCID 54076911N1-[2-(4-cyanophenoxy)-1-methylethyl]-N2-(4-methylbenzyloxycarbonyl)-L-valinamideAusbeute 25,1 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
-20 °C

Versuchsvorschrift

0.6 g of N-methylpiperidine was added to a solution containing 1.5 g of N-(4-methylbenzyloxycarbonyl)-L-valine dissolved in 100 ml of methylene chloride, at -20° C. After the mixture was stirred for 10 minutes at the same temperature, 0.8 g of isobutyl chloroformate was added to the mixture, and stirred for 1 hour at -20° C. 1.0 g of 2-(4-cyanophenoxy)-1-methylethylamine was added to this mixture at -60° C., and then the reaction mixture was allowed to sit and warm naturally to room temperature while being stirred, and was stirred for 20 hours at room temperature. Water was subsequently added to the reaction mixture. After the methylene chloride layer was washed successively with a 5% aqueous solution of sodium bicarbonate and water, the organic layer was dried over anhydrous magnesium sulfate and the methylene chloride was removed under reduced pressure. The residue, which was a crude crystal, was purified by column chromatography on silica gel, thus obtaining 0.6 g of the desired product in the form of light white powder (yield: 28%).

Aufarbeitung

  1. additionwas added to the mixture
  2. temperaturewarm naturally to room temperature
  3. stirringwhile being stirred
  4. stirringwas stirred for 20 hours at room temperature
  5. washAfter the methylene chloride layer was washed successively with a 5% aqueous solution of sodium bicarbonate and water
  6. dry with materialthe organic layer was dried over anhydrous magnesium sulfate
  7. customthe methylene chloride was removed under reduced pressure
  8. customwas purified by column chromatography on silica gel

Quellen und Nachweise

ORD-Eintrag
ord-218372b1aeb94ade8dabbdf60b32ad27
Quelldatensatz
uspto-grants-1996_11
Patentnummer
US05574064

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