Identification | Back Directory | [Name]
3-Amino-3-iminopropanoic acid ethyl ester hydrochloride | [CAS]
57508-48-2 | [Synonyms]
ETHYL AMIDINOACETATE HCL 2-Amidinoacetate HydrochL Ethyl amidinoacetate hydrochloride carbethoxyacetamidine hydrochloride Ethyl 2-Amidinoacetate Hydrochloride ethyl 2-carbaMiMidoylacetate hydrochloride Ethyl3-amino-3-iminopropanoate hydrochloride Ethyl 3-aMino-3-iMinopropanate hydrochloride 1-amino-3-ethoxy-3-oxopropan-1-iminium chloride 3-AMINO-3-IMINO-PROPANOIC ACID, ETHYL ESTER HCL CARBAMIMIDOYL-ACETIC ACID ETHYL ESTER HYDROCHLORIDE 3-amino-3-imiopropanoic acid ethyl ester hydrochloride 3-AMINO-3-IMINOPROPIONIC ACID ETHYL ESTER HYDROCHLORIDE 3-Amino-3-iminopropanoic acid ethyl ester hydrochloride Propanoic acid, 3-aMino-3-iMino-, ethyl ester, hydrochloride 3-amino-3-imino-Propanoic acid ethyl ester hydrochloride (1:1) Propanoic acid, 3-aMino-3-iMino-, ethyl ester, hydrochloride (1:1) | [Molecular Formula]
C5H11ClN2O2 | [MDL Number]
MFCD06797615 | [MOL File]
57508-48-2.mol | [Molecular Weight]
166.61 |
Chemical Properties | Back Directory | [Melting point ]
105-108℃ | [storage temp. ]
Inert atmosphere,Room Temperature | [form ]
Solid | [Appearance]
White to light yellow Solid | [InChI]
InChI=1S/C5H10N2O2.ClH/c1-2-9-5(8)3-4(6)7;/h2-3H2,1H3,(H3,6,7);1H | [InChIKey]
VOHFLYOSVGWQOS-UHFFFAOYSA-N | [SMILES]
C(C(OCC)=O)C(N)=N.Cl |
Hazard Information | Back Directory | [Uses]
It is used as a pharmaceutical intermediate. | [Synthesis]
The general procedure for the synthesis of ethyl 3-amidinopropionate hydrochloride from ethyl 3-ethoxy-3-iminopropionate was as follows: ethyl 3-amino-3-ethoxyacrylate (760 mg, 4.78 mmol) and ammonium chloride (270 mg, 5.0 mmol) were dissolved in ethanol (4.0 mL) in a glass tube rated for 10 mL pressure. The reaction was carried out using a CEM Discover microwave synthesizer at an initial magnetron power of 200 W for 1 h at 120°C (hold time). Upon completion of the reaction, the reaction mixture was cooled in a stream of compressed air and subsequently filtered. The filtrate was concentrated by vacuum evaporation and the residue was ground with diethyl ether to afford ethyl 3-amidinopropionate hydrochloride (923 mg, 78% yield) as a colorless solid, which was ready for use without further purification. The product characterization data were as follows: νmax (neat)/ cm-1 3300, 3095, 1738, 1687; δH (500 MHz; d6-DMSO)/ ppm 9.16 (2H, broad single peak, NH2), 8.88 (2H, broad single peak, NH2), 4.15 (2H, quartet peak, J = 7.1 Hz, OCH2), 3.63 (2H, single peak, CH2), 1.22 (3H, triple peak, J = 7.1 Hz, CH3); δC (125 MHz, d6-DMSO)/ ppm 166.7 (C=O), 163.6 (C=N), 61.9 (OCH2), 38.2 (CH2), 14.4 (CH3); m/z (EI) 130 (M-+). | [References]
[1] Synlett, 2016, vol. 27, # 11, p. 1728 - 1732 [2] Chemical and Pharmaceutical Bulletin, 1995, vol. 43, # 5, p. 788 - 796 [3] Patent: WO2008/33745, 2008, A2. Location in patent: Page/Page column 70 [4] Patent: WO2008/33747, 2008, A2. Location in patent: Page/Page column 254-255 [5] European Journal of Medicinal Chemistry, 2011, vol. 46, # 12, p. 6002 - 6014 |
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