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5-ETHYL-2-THIOURACIL

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5-ETHYL-2-THIOURACIL Basic information

Product Name:
5-ETHYL-2-THIOURACIL
Synonyms:
  • 5-ETHYL-2-THIOURACIL
  • 5-Ethyl-2-thiouracil ,98%
  • 5-ethyl-2-sulfanylidene-1,2,3,4-tetrahydropyriMidin-4-one
  • 5-Ethyl-2-thioxo-2,3-dihydropyriMidin-4(1H)-one
  • 4(1H)-Pyrimidinone, 5-ethyl-2,3-dihydro-2-thioxo-
  • 5-ETHYL-2-THIOURACIL USP/EP/BP
CAS:
34171-37-4
MF:
C6H8N2OS
MW:
156.21
Mol File:
34171-37-4.mol
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5-ETHYL-2-THIOURACIL Chemical Properties

Melting point:
191-193℃
Density 
1.29±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
DMSO (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form 
Solid
pka
7.69±0.25(Predicted)
color 
Pale Yellow to Pale Beige
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Safety Information

WGK Germany 
3
HS Code 
29335990

MSDS

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5-ETHYL-2-THIOURACIL Usage And Synthesis

Chemical Properties

Off-white solid

Uses

5-Ethyl-2-thiouracil is a modified nucleobase and a versatile reactant used in the synthesis. It was used as a reactant in the inhibition of Hepatitis B virus (HBV) replication.

Synthesis

105-54-4

17356-08-0

109-94-4

34171-37-4

Step D75: Synthesis of 5-ethyl-2-thio-2,3-dihydro-4(1H)-pyrimidinone 1. To a suspension of potassium tert-butanolate (12.08 g, 108 mmol) in THF (40 mL) under nitrogen protection was slowly added dropwise a mixed solution of ethyl butyrate (5.69 mL, 43.0 mmol) and ethyl formate (6.93 mL, 86 mmol) in ether (40.0 mL). 2. The reaction mixture was stirred at room temperature for 3 hours. 3. Upon completion of the reaction, the solvent was removed under reduced pressure to give an oily residue. 4. The residue was dissolved in isopropanol (350 mL) and thiourea (6.55 g, 86 mmol) was added. 5. The mixture was heated to reflux and stirred overnight. 6. At the end of the reaction, the reaction solution was concentrated under vacuum to give a solid product. 7. The solid product was dissolved in water and the pH was adjusted to 4 with acetic acid (AcOH). 8. 8. The aqueous phase was extracted with dichloromethane (DCM) and the organic layers were combined. 9. The organic layer was dried with anhydrous sodium sulfate (Na2SO4), filtered and concentrated under reduced pressure to give 5-ethyl-2-thiouracil (5.5 g, 82% yield) as a pink solid.

References

[1] Patent: WO2012/76435, 2012, A1. Location in patent: Page/Page column 49

5-ETHYL-2-THIOURACIL Preparation Products And Raw materials

Raw materials

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