Carbon Dioxide → HCID 140522022, compound

HRID 1788324Notes

Reaction equation

HRID 1788324 reaction equation
[C:1](Cl)(=[O:13])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[O:15]=[C:16]([CH2:18][N:19]([C:21](=[NH:23])[NH2:22])[CH3:20])[OH:17].N1C=CC=CC=1.C(=O)=O>ClCCl.CC(C)=O>[C:1]([NH:23][C:21](=[NH:22])[N:19]([CH2:18][C:16]([OH:17])=[O:15])[CH3:20])(=[O:13])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]

Participants

7

Reactant 4

HCID 280Carbon DioxideHCID 586CreatineHCID 1049PyridineHCID 8166Dodecanoyl chloride4×

Product 1

HCID 140522022HCID 140522022, compound

Reagents, catalysts & solvents 2

HCID 180AcetoneSolventHCID 6344DichloromethaneSolvent

Procedure

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 dodecanoyl chloride solution, 7.34 g (56 mmol) of creatine is suspended, with stirring, in 50 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 about −15° C. and 0° C. When the target temperature is reached the drop wise addition of dodecanoyl chloride is commenced. Addition of dodecanoyl chloride continues, with cooling and stirring, until all of the dodecanoyl chloride 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-(3-dodecanoyl-1-methylguanidino)acetic acid.

Workup

  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

Sources & evidence

ORD record
ord-f97a24765fae4e6bb2fa83918acd3402
Source dataset
uspto-grants-2009_03
Patent number
US07511163B2

Reaction notes

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