ChemicalBook--->CAS DataBase List--->57508-48-2

57508-48-2

57508-48-2 Structure

57508-48-2 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Hazard InformationBack Directory
[Uses]

It is used as a pharmaceutical intermediate.
[Synthesis]

ethyl 3-ethoxy-3-iminopropionate

27317-59-5

3-Amino-3-iminopropanoic acid ethyl ester hydrochloride

57508-48-2

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
Spectrum DetailBack Directory
[Spectrum Detail]

3-Amino-3-iminopropanoic acid ethyl ester hydrochloride(57508-48-2)1HNMR
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