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3-Amino-2-oxazolidinone

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3-Amino-2-oxazolidinone manufacturers

3-Amino-2-oxazolidinone Basic information
Product Name:3-Amino-2-oxazolidinone
Synonyms:3-Amino-1,3-oxazolidin-2-one;NSC 111187;NSC 196570;NSC 38250;3-AMINO-OXAZOLIDINONE;3-azanyl-1,3-oxazolidin-2-one;AOZ,3-Amino-2-oxazolidinone;3-Amino-2-oxazolidinone AOZ
CAS:80-65-9
MF:C3H6N2O2
MW:102.09
EINECS:201-299-2
Product Categories:Heterocycles;VARIOUSAMINE;Isoxazoles, Oxadiazoles, Oxazoles;Various Metabolites and Impurities;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals
Mol File:80-65-9.mol
3-Amino-2-oxazolidinone Structure
3-Amino-2-oxazolidinone Chemical Properties
Melting point 65-67 °C
Boiling point 135 °C(Press: 0.7 Torr)
density 1.179
storage temp. Keep in dark place,Sealed in dry,2-8°C
solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form Solid
pka3.24±0.20(Predicted)
color White to Off-White
BRN 109430
InChIInChI=1S/C3H6N2O2/c4-5-1-2-7-3(5)6/h1-2,4H2
InChIKeyKYCJNIUHWNJNCT-UHFFFAOYSA-N
SMILESO1CCN(N)C1=O
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36/37
WGK Germany 3
HS Code 29349990
MSDS Information
3-Amino-2-oxazolidinone Usage And Synthesis
Chemical PropertiesWhite Solid
UsesA metabolite of Furazolidone and Nitrofuran. Environmental contaminants; Food contaminants; Heat processing contaminants
DefinitionChEBI: 3-Amino-2-oxazolidone is an oxazolidinone.
Synthesis
2-Hydroxyethylhydrazine

109-84-2

Diethyl carbonate

105-58-8

3-AMINO-2-OXAZOLIDINONE

80-65-9

General procedure for the synthesis of 3-aminooxazolidin-2-one from 2-hydrazinoethanol and diethyl carbonate: 15.2 g (0.2 mol) of 2-hydrazinoethanol (Intermediate 1), 31.0 g (0.2 mol) of diethyl carbonate, and 3.0 g (57 mmol) of sodium methanol were added to a 100 mL three-necked flask, and the mixture was heated and refluxed for 4 hours. Upon completion of the reaction, the reaction mixture was cooled and a solid was precipitated. The solid was collected by vacuum filtration and dried. The solvent in the mother liquor was removed by distillation. The crude product was purified by column chromatography (eluent: methanol/dichloromethane, 1:20, v/v), and the resulting white solid was recrystallized in ethanol to give 15.3 g of 3-aminooxazolidin-2-one (Intermediate 2) in 75% yield. The product was characterized as follows: 1H-NMR (400 MHz, D2O) δ ppm: 4.33 (2H, t, J = 8.0 Hz), 3.94 (2H, s), 3.70 (2H, t, J = 4.0 Hz); EI-MS (m/z): 103.1 [M + H]+; Melting point: 64-66 °C.

References[1] Patent: EP2952509, 2015, A1. Location in patent: Paragraph 0043; 0044
[2] Journal of the American Chemical Society, 1955, vol. 77, p. 2277,2280, 2281
[3] Journal of the American Chemical Society, 1977, vol. 99, p. 1172 - 1180
[4] Journal of the Chemical Society, 1963, p. 3523 - 3528
[5] Journal of Organic Chemistry, 1966, vol. 31, p. 631 - 632
3-Amino-2-oxazolidinone Preparation Products And Raw materials
Raw materials2-Hydroxyethylhydrazine-->NSC 206120-->Furazolidone-->Diethyl carbonate
Tag:3-Amino-2-oxazolidinone(80-65-9) Related Product Information
Famoxadone 2-NP-AOZ Moxnidazole Morphlinomethyl-3-[(5-nitrofurfurylidene)-amino]-2-oxazolidinone Oxadixyl Nifuratel Furazolidone D-Cycloserine PHENSUXIMIDE Furaltadone 3-Amino-2-oxazolidinone 3-Amino-5-morpholinomethyl-2-oxazolidinone 5-(4-Morpholinylmethyl-d8)-3-[[(5-nitro-2-furanyl)methylene]amino]-2-oxazolidinone 5-(4-Ethyl-1-piperazinyl)methyl-3-(5-nitrofurfurylidene)amino-2-oxazolidinone 2-NP-AOZ-D4 3-Amino-2-oxazolidinone d4 5-Morpholinomethyl-3-[5-nitrofurfurylideneamino]-2-oxazolidinone tartrate salt 3-Amino-2-oxazolidinone sulfate