N-CARBOXYETHYLRHODANINE

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N-CARBOXYETHYLRHODANINE Basic information
Product Name:N-CARBOXYETHYLRHODANINE
Synonyms:3-Thiazolidinepropanoic acid, 4-oxo-2-thioxo-;3-Thiazolidinepropionic acid, 4-oxo-2-thioxo-;4-oxo-2-thioxo-3-thiazolidinepropionicaci;Rodanin-3-propionic acid;rodanin-3-propionicacid;AKOS BBS-00002147;3-(4-OXO-2-THIOXO-1,3-THIAZOLIDIN-3-YL)PROPANOIC ACID;3-(4-OXO-2-THIOXO-THIAZOLIDIN-3-YL)-PROPIONIC ACID
CAS:7025-19-6
MF:C6H7NO3S2
MW:205.25
EINECS:230-307-7
Product Categories:
Mol File:7025-19-6.mol
N-CARBOXYETHYLRHODANINE Structure
N-CARBOXYETHYLRHODANINE Chemical Properties
Melting point 158-160°C
Boiling point 385.9±44.0 °C(Predicted)
density 1.61±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form powder to crystal
pka4.36±0.10(Predicted)
color Light yellow to Brown
CAS DataBase Reference7025-19-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36/37/39
RTECS XJ6094060
HS Code 2934.10.9000
HazardClass IRRITANT
MSDS Information
N-CARBOXYETHYLRHODANINE Usage And Synthesis
Synthesis
Carbon disulfide

75-15-0

Bromoacetic acid

79-08-3

β-Alanine

107-95-9

N-CARBOXYETHYLRHODANINE

7025-19-6

Synthesis of 3-(4-oxo-2-thioxothiazolidin-3-yl)propionic acid (33): β-alanine 32 (3.4 g, 38.1 mmol) was dissolved in 17 mL of 22% potassium hydroxide solution, and the temperature of the reaction was controlled not to exceed 25 °C. Carbon disulfide (2.5 mL, 42 mmol) was added slowly and dropwise. The reaction mixture was stirred at room temperature. Subsequently, batchwise addition of bromoacetic acid (5.3 g, 38.1 mmol) was made over about 20 minutes, and the whole process was completed in about 3 hours. After addition, stirring was continued at room temperature for 3 hours, during which precipitation was observed. The pH of the reaction mixture was adjusted with concentrated hydrochloric acid to 3-4. After addition of sulfuric acid, the solution was stirred at room temperature overnight. The precipitate was collected by filtration and washed with water to give pure target compound 33 (3.52 g, 45% yield) as a yellow solid. Melting point 155-156 °C. 1H NMR (400 MHz, MeOD-d4) δ (ppm): 5.00 (brs, 1H), 4.22 (t, J = 7.5 Hz, 2H), 4.11 (s, 1H), 2.64 (t, J = 7.6 Hz, 2H). 13C NMR (100 MHz, MeOD-d4) δ (ppm): 202.58, 174.37, 172.87, 39.64, 35.08, 30.28. mass spectrum (ESI) m/z: 204.1 [M-H]+. Elemental analysis (C6H7NO3S2) Calculated values: C, 35.11; H, 3.44; N, 6.82. Measured values: C, 35.10; H, 3.48; N, 6.88.

References[1] ChemMedChem, 2014, vol. 9, # 11, p. 2538 - 2547
[2] Patent: WO2011/39735, 2011, A2. Location in patent: Page/Page column 149-150
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