Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyrimidines >  Thio pyrimidine >  Ethanone, 1-[2-(methylthio)-4-pyrimidinyl]- (9CI)

Ethanone, 1-[2-(methylthio)-4-pyrimidinyl]- (9CI)

Basic information Safety Supplier Related

Ethanone, 1-[2-(methylthio)-4-pyrimidinyl]- (9CI) Basic information

Product Name:
Ethanone, 1-[2-(methylthio)-4-pyrimidinyl]- (9CI)
Synonyms:
  • Ethanone, 1-[2-(methylthio)-4-pyrimidinyl]- (9CI)
  • 1-[2-(Methylthio)-4-pyrimidinyl]ethanone
  • 1-(2-(Methylthio)pyrimidin-4-yl)ethanone
  • 1-[2-(Methylsulfanyl)-4-pyrimidinyl]-1-ethanone
  • 4-Acetyl-2-methylthiopyrimidine
  • 1-(2-Methylsulfanyl-pyriMidin-4-yl)-ethanone
  • 1-[2-(Methylsulfanyl)pyriMidin-4-yl]ethan-1-one
  • 1-[2-(Methylsulfanyl)pyriMidin-4-yl]-1-ethanone
CAS:
496863-48-0
MF:
C7H8N2OS
MW:
168.22
EINECS:
200-589-5
Product Categories:
  • ACETYLGROUP
Mol File:
496863-48-0.mol
More
Less

Ethanone, 1-[2-(methylthio)-4-pyrimidinyl]- (9CI) Chemical Properties

Boiling point:
301℃
Density 
1.23
Flash point:
136℃
storage temp. 
Inert atmosphere,Room Temperature
pka
-1.05±0.20(Predicted)
Appearance
White to off-white Solid
InChI
InChI=1S/C7H8N2OS/c1-5(10)6-3-4-8-7(9-6)11-2/h3-4H,1-2H3
InChIKey
WXQMROLQWGTVBM-UHFFFAOYSA-N
SMILES
C(=O)(C1C=CN=C(SC)N=1)C
More
Less

Safety Information

HazardClass 
IRRITANT
HS Code 
2933599590
More
Less

Ethanone, 1-[2-(methylthio)-4-pyrimidinyl]- (9CI) Usage And Synthesis

Synthesis

75-97-8

4637-24-5

17356-08-0

74-88-4

496863-48-0

1) Synthesis of 4-acetyl-2-methylthiopyrimidine: 3,3-dimethylbutan-2-one (25.15 g) was mixed with N,N-dimethylformamide dimethyl acetal (126 mL) and stirred in an oil bath at 100 °C for 48 hours. Upon completion of the reaction, the reaction was air cooled and the low-boiling component was removed by distillation under reduced pressure. Methanol (400 mL), thiourea (28.92 g) and sodium methanol (15.39 g) were added to the residue and heated to reflux for 118 hours. After air cooling again, sodium methanol (10.26 g) was added and under ice bath cooling, iodomethane (17.8 mL) was added dropwise over 5 minutes and stirring was continued for 5 hours. After completion of the reaction, the solvent was removed by concentration under reduced pressure and the residue was partitioned with water and ethyl acetate. The organic layer was washed sequentially with water and saturated saline and dried over anhydrous sodium sulfate. After filtration, it was concentrated under reduced pressure and the residue was dissolved in 3N aqueous hydrochloric acid (400 mL) and stirred at room temperature for 15 hours. The reaction solution was extracted with ethyl acetate, the organic layer was dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: ethyl acetate-hexane) to afford 4-acetyl-2-methylthiopyrimidine (26.34 g, 82% yield) as a solid.1H-NMR (400 MHz, CDCl3) δ: 2.63 (3H, s), 2.70 (3H, s), 7.51 (1H, d, J = 4.9 Hz), 8.74 (1H , d, J = 4.9 Hz).ESI-MS m/z: 169 ([M + H]+).

References

[1] Patent: EP1785418, 2007, A1. Location in patent: Page/Page column 39

Ethanone, 1-[2-(methylthio)-4-pyrimidinyl]- (9CI)Supplier

Jinan Xinzheng Pharmaceutical Technology Co., Ltd. Gold
Tel
0531-88798968 18615218958
Email
yin3684895@126.com
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Email
sales@chemwish.com
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18
Shanghai Sinch Parmaceuticals Tech. Co. Ltd.
Tel
+86-21-54098501
Email
sales@sinch.com.cn
More
Less

Ethanone, 1-[2-(methylthio)-4-pyrimidinyl]- (9CI)(496863-48-0)Related Product Information