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    ChemicalBook CAS DataBase List DL-Homocysteine
    454-29-5

    DL-Homocysteine synthesis

    5synthesis methods
    -

    Yield:454-29-5 36 %Chromat. ,462-10-2 14 %Chromat.

    Reaction Conditions:

    with sodium sulfide;carbon dioxide in 1-methyl-pyrrolidin-2-one at 20 - 90; for 0.666667 h;

    Steps:

    3 EXAMPLE 3 Preparation of Homocysteine According to the Invention
    EXAMPLE 3 Preparation of Homocysteine According to the Invention With the method of the invention, it is also possible to obtain the dimer of homocysteine (called homocystine). [0033] This example is carried out on a scale of 1 mmol of 2ABL in a pill box with magnetic stirring. The 2-ABL is placed in solution in 1.2 mL of NMP. CO2 bubbling is carried out at 20° C. for 10 mins, and then 10.8 mL of NMP and 3 equivalents of Na2S are added. The reaction medium placed under stirring is gradually heated up to 90° C. After 30 mins, the medium is hydrolyzed by simple dilution in the HPLC solvent. [0034] These conditions allow formation of homocysteine and of its dimer. The best performances are obtained at a temperature of 90° C. [0035] After a reaction time of 30 mins, the reaction is completed. At a higher temperature and in the presence of 3 equivalents of Na2S, homocystine is favored. Excess Na2S accelerates dimerization of homocysteine. [0036] The following yields (HPLC) are obtained: Homocysteine 36% Homocystine 14% Diketopiperazine 2%

    References:

    ADISSEO FRANCE S.A.S.;Huet, Robert;Joerger, Jean-Michel;Henryon, Vivien US2013/184474, 2013, A1 Location in patent:Paragraph 0031; 0032; 0033; 0034; 0035; 0036

    FullText

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