Carbon Dioxide → HCID 140522019, Verbindung

HRID 1788326Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1788326
[C:1](Br)(=[O:17])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16].[O:19]=[C:20]([CH2:22][N:23]([C:25](=[NH:27])[NH2:26])[CH3:24])[OH:21].N1C=CC=CC=1.C(=O)=O>ClCCl.CC(C)=O>[CH3:24][N:23]([CH2:22][C:20]([OH:21])=[O:19])[C:25]([NH:27][C:1](=[O:17])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])=[NH:26]

Komponenten

7

Versuchsvorschrift

In a dry 3-necked, round bottomed flask, equipped with a magnetic stirrer, a thermometer, a nitrogen inlet tube and the dropping funnel containing the palmitoyl bromide solution, 10.99 g (60 mmol) of creatine is suspended, with stirring, in 100 ml of dry dichloromethane. To this suspension a catalytic amount (0.1 mmol) of pyridine is also added. The suspension is stirred in a dry ice and acetone bath to a temperature of between to about −10° C. and 0° C. When the target temperature is reached the drop wise addition of palmitoyl bromide is commenced. Addition of palmitoyl bromide continues, with cooling and stirring, until all of the palmitoyl bromide is added, after which the reaction is allowed to warm to room temperature with constant stirring. The solution is then filtered to remove any remaining creatine and the volatile dichloromethane and pyridine are removed under reduced pressure yielding 2-(1-methyl-3-palmitoylguanidino)acetic acid.

Aufarbeitung

  1. customIn a dry 3-necked, round bottomed flask, equipped with a magnetic stirrer
  2. temperaturewith cooling
  3. filtrationThe solution is then filtered
  4. customto remove any remaining creatine
  5. customthe volatile dichloromethane and pyridine are removed under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-c7baff985f1c4b459347dff42e8198b7
Quelldatensatz
uspto-grants-2009_03
Patentnummer
US07511163B2

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