Diethyl acetamidomalonate

Diethyl acetamidomalonate
Identifiers
CAS Number	1068-90-2;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL3278808;
ChemSpider	13422;
ECHA InfoCard	100.012.685
EC Number	213-952-9;
PubChem CID	14041;
UNII	4VDX81E00W;
CompTox Dashboard (EPA)	DTXSID6061446 ;
	InChI InChI=1S/C9H15NO5/c1-4-14-8(12)7(10-6(3)11)9(13)15-5-2/h7H,4-5H2,1-3H3,(H,10,11) Key: ISOLMABRZPQKOV-UHFFFAOYSA-N;
	SMILES CCOC(=O)C(C(=O)OCC)NC(=O)C;
Properties
Chemical formula	C9H15NO5
Molar mass	217.22 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Diethyl acetamidomalonate (DEAM) is a derivative of malonic acid diethyl ester. Formally, it is derived through the acetylation of ester from the unstable aminomalonic acid. DEAM serves as a starting material for racemates including both, natural and unnatural α-amino acids or hydroxycarboxylic acids. It is also usable as a precursor in pharmaceutical formulations, particularly in the cases of active ingredients like fingolimod, which is used to treat multiple sclerosis.

Occurrence and preparation

A notable method for synthesizing acetamidomalon ester is described in a 1950 patent,^[1] which cites a procedure previously featured in Organic Syntheses.^[2] The synthesis procedure involves the preparation of malonic acid diethyl ester in acetic acid combined with sodium nitrite (NaNO₂), resulting in diethyl isonitrosomalonate (also known as α-oximinomalonic acid diethyl ester).

The process further involves reducing a solution of this intermediate in a mixture of glacial acetic acid and acetic anhydride using zinc powder. The resulting amine is then combined with acetic anhydride to produce the final product DEAM, achieving a total yield of 77% acetylation.

Properties

Diethyl acetamidomalonate is a white powdery substance characterized by low water solubility, but possessing good solvency in lower alcohols and chloroform.

Applications

Synthesis of α-amino acids

Acetamidomalonic acid diethyl ester can be viewed as a achiral glycine with a protecting group. DEAM comprises a malonic acid diethyl ester structure, making it suitable for malonic ester synthesis. In a three-step process, the synthesis involves deprotonation, alkylation, hydrolysis, and simultaneous decarboxylation, resulting in racemic α-amino acids.

Thus, phenylalanine (rac-Phe) can be produced by alkylating DEAM using benzyl chloride in the presence of sodium ethoxide (NaOEt). Hydrolysis of the carboxylic acid ester and amide functions then follows along with decarboxylation at increased temperatures. This gives the monocarboxylic acid with a 65% yield.^[3]^[4]

The oxidation-sensitive amino acid rac-tryptophan can be synthesized using diethyl acetamidomalonate and gramine, or through its quaternary ammonium compound which can be obtained with methyl iodide or dimethyl sulfate, yielding results of > 90%.^[5]^[6]

Alkylation of acetamidomalon diethyl ester can also be carried out using propiolactone, showcasing a high reactivity towards nucleophilicity. This process results in the formation of racemic glutamic acid in a one-pot reaction, yielding 87% .^[7]

The method can also be applied to synthesize non-natural α-amino acids, such as those with heterocyclic substituents.^[8] The methylene group of diethyl acetamidomalonate can undergo a polarity reversal when DEAM is converted into the dehydroform. This compound can be nucleophilically attacked by organolithium compounds, Grignard compounds, or malonic ester anions.^[9]

conversion of diethyl acetamidomalonate

Synthesis of α-hydroxycarboxylic acids

The amino group in synthetic α-amino acids can be replaced by a hydroxy group through diazotization and overcooking.

An alkyne-carboxylic acid, such as 2-hydroxy-4-pentanoic acid, that can be obtained through this method, can undergo copolymerization with lactic acid. The resulting bonds of alkyne residues that are attached to the polymer chain in the acquired polylactide copolymer can then be made to undergo a cycloaddition with functional organic azides in order to create 1,2,3-triazoles. This process falls under the category of click chemistry, known for mild and smooth reactions.^[10]

Syntheses of fingolimod

For the production of Fingolimod—an immunosuppressant used to treat multiple sclerosis, numerous synthetic routes have been developed utilizing diethyl acetamidomalonate as the principal component.^[11] The key step in these multistep synthesis processes involves typically the alkylation of DEAM with, for example, 4'-(2-iodoethyl)octanophenone.^[12]

.

References

^ US 2521809, M. Tishler, E.E. Howe, "Preparation of acetamidomalonates", published 1950-9-12, assigned to Merck & Co., Inc.
^ "Diethyl Acetamidomalonate". Organic Syntheses. doi:10.15227/orgsyn.040.0021.
^ N.F. Albertson, S. Archer (1945), "The use of ethyl acetamidomalonate in the synthesis of amino acids. The preparation of dl-histidine, dl-phenylalanine and dl-leucine", J. Amer. Chem. Soc., vol. 67, no. 2, pp. 308–310, doi:10.1021/ja01218a046
^ H.R. Snyder, J.F. Shekleton, C.D. Lewis (1945), "Synthetic aminoacids. Syntheses from acetamidomalonic esters", J. Amer. Chem. Soc., vol. 67, no. 2, pp. 310–312, doi:10.1021/ja01218a047{{citation}}: CS1 maint: multiple names: authors list (link)
^ N.F. Albertson, S. Archer, C.M. Suter (1945), "The synthesis of tryptophan from gramine", J. Amer. Chem. Soc., vol. 67, no. 1, pp. 36–37, doi:10.1021/ja01217a010{{citation}}: CS1 maint: multiple names: authors list (link)
^ E.E. Howe, A.J. Zambito, H.R. Snyder, M. Tishler (1945), "The application of a new alkylation reaction to the synthesis of tryptophan", J. Amer. Chem. Soc., vol. 67, no. 1, pp. 38–39, doi:10.1021/ja01217a011{{citation}}: CS1 maint: multiple names: authors list (link)
^ G. Talbot, R. Gaudry, L. Berlinguet (1956), "A convenient synthesis of DL-glutamic acid from β-propiolactone", Can. J. Chem., vol. 34, no. 10, pp. 1440–1443, doi:10.1139/v56-184{{citation}}: CS1 maint: multiple names: authors list (link)
^ P.N. Rao, J.E. Burdett,Jr., J.W. Cessac, C.M. DiNunno, D.M. Peterson, H.K. Kim (1987), "Synthesis of 3-(3-pyridyl)- and 3-(3-benzo[b]thienyl)-D-alanine", Int. J. Pept. Protein Res., vol. 29, no. 1, pp. 118–125, doi:10.1111/j.1399-3011.1987.tb02237.x, PMID 3570651{{citation}}: CS1 maint: multiple names: authors list (link)
^ F. Effenberger, T. Beißwenger (1982), "Eine einfache, allgemein anwendbare Synthese von N-Acetyl-dehydro-α-aminosäuren", Angew. Chem., vol. 94, no. 3, p. 210, Bibcode:1982AngCh..94..210E, doi:10.1002/ange.19820940316
^ Q. Zhang, H. Ren, G.L. Baker (2014), "An economical and safe procedure to synthesize 2-hydroxy-4-pentynoic acid: A precursor towards 'clickable' biodegradable polylactide", Beilstein J. Org. Chem., vol. 10, pp. 1365–1371, doi:10.3762/bjoc.10.139, PMC 4077406, PMID 24991290, S2CID 11575521{{citation}}: CS1 maint: multiple names: authors list (link)
^ N. Mulakayala (2016), "A comprehensive review on synthetic approach for Fingolimod" (PDF), IJACS, vol. 4, no. 4, pp. 362–366
^ EP 0989113, S. Hirase, S. Sasaki, M. Yoneta, R. Hirose, T. Fujita, "Processes for producing 2-aminomalonic acid derivatives and 2-amino-1,3-propanediol derivatives, and intermediates for producing the derivatives", published 2000-03-29, assigned to Taito Co., Ltd.

[1] US 2521809, M. Tishler, E.E. Howe, "Preparation of acetamidomalonates", published 1950-9-12, assigned to Merck & Co., Inc.

[2] "Diethyl Acetamidomalonate". Organic Syntheses. doi:10.15227/orgsyn.040.0021.

[3] N.F. Albertson, S. Archer (1945), "The use of ethyl acetamidomalonate in the synthesis of amino acids. The preparation of dl-histidine, dl-phenylalanine and dl-leucine", J. Amer. Chem. Soc., vol. 67, no. 2, pp. 308–310, doi:10.1021/ja01218a046

[4] H.R. Snyder, J.F. Shekleton, C.D. Lewis (1945), "Synthetic aminoacids. Syntheses from acetamidomalonic esters", J. Amer. Chem. Soc., vol. 67, no. 2, pp. 310–312, doi:10.1021/ja01218a047{{citation}}: CS1 maint: multiple names: authors list (link)

[5] N.F. Albertson, S. Archer, C.M. Suter (1945), "The synthesis of tryptophan from gramine", J. Amer. Chem. Soc., vol. 67, no. 1, pp. 36–37, doi:10.1021/ja01217a010{{citation}}: CS1 maint: multiple names: authors list (link)

[6] E.E. Howe, A.J. Zambito, H.R. Snyder, M. Tishler (1945), "The application of a new alkylation reaction to the synthesis of tryptophan", J. Amer. Chem. Soc., vol. 67, no. 1, pp. 38–39, doi:10.1021/ja01217a011{{citation}}: CS1 maint: multiple names: authors list (link)

[7] G. Talbot, R. Gaudry, L. Berlinguet (1956), "A convenient synthesis of DL-glutamic acid from β-propiolactone", Can. J. Chem., vol. 34, no. 10, pp. 1440–1443, doi:10.1139/v56-184{{citation}}: CS1 maint: multiple names: authors list (link)

[8] P.N. Rao, J.E. Burdett,Jr., J.W. Cessac, C.M. DiNunno, D.M. Peterson, H.K. Kim (1987), "Synthesis of 3-(3-pyridyl)- and 3-(3-benzo[b]thienyl)-D-alanine", Int. J. Pept. Protein Res., vol. 29, no. 1, pp. 118–125, doi:10.1111/j.1399-3011.1987.tb02237.x, PMID 3570651{{citation}}: CS1 maint: multiple names: authors list (link)

[9] F. Effenberger, T. Beißwenger (1982), "Eine einfache, allgemein anwendbare Synthese von N-Acetyl-dehydro-α-aminosäuren", Angew. Chem., vol. 94, no. 3, p. 210, Bibcode:1982AngCh..94..210E, doi:10.1002/ange.19820940316

[10] Q. Zhang, H. Ren, G.L. Baker (2014), "An economical and safe procedure to synthesize 2-hydroxy-4-pentynoic acid: A precursor towards 'clickable' biodegradable polylactide", Beilstein J. Org. Chem., vol. 10, pp. 1365–1371, doi:10.3762/bjoc.10.139, PMC 4077406, PMID 24991290, S2CID 11575521{{citation}}: CS1 maint: multiple names: authors list (link)

[11] N. Mulakayala (2016), "A comprehensive review on synthetic approach for Fingolimod" (PDF), IJACS, vol. 4, no. 4, pp. 362–366

[12] EP 0989113, S. Hirase, S. Sasaki, M. Yoneta, R. Hirose, T. Fujita, "Processes for producing 2-aminomalonic acid derivatives and 2-amino-1,3-propanediol derivatives, and intermediates for producing the derivatives", published 2000-03-29, assigned to Taito Co., Ltd.

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