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ETHYL 2-(METHYLSULFONYL)PYRIMIDINE-5-CARBOXYLATE

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ETHYL 2-(METHYLSULFONYL)PYRIMIDINE-5-CARBOXYLATE Basic information

Product Name:
ETHYL 2-(METHYLSULFONYL)PYRIMIDINE-5-CARBOXYLATE
Synonyms:
  • 2-(Methylsulfonyl)-5-pyrimidinecarboxylic acid ethyl ester
  • ETHYL 2-(METHYLSULFONYL)PYRIMIDINE-5-CARBOXYLATE
  • ETHYL 2-(METHYLSULPHONYL)PYRIMIDINE-5-CARBOXYLATE
  • Ethyl 2-(methylsulfonyl)pyrimidine-5-carboxylate 95%
  • 5-Pyrimidinecarboxylic acid, 2-(methylsulfonyl)-, ethyl ester
  • ETHYL 2-(METHYLSULFONYL)PYRIMIDINE-5-CARBOXYLATE ISO 9001:2015 REACH
  • Ethyl 2-(Methylsulfonyl)-5-pyrimidinecarboxylate
CAS:
148550-51-0
MF:
C8H10N2O4S
MW:
230.24
Product Categories:
  • Pyridines, Pyrimidines, Purines and Pteredines
Mol File:
148550-51-0.mol
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ETHYL 2-(METHYLSULFONYL)PYRIMIDINE-5-CARBOXYLATE Chemical Properties

Boiling point:
407.7±37.0 °C(Predicted)
Density 
1.338±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
-4.99±0.22(Predicted)
Appearance
Off-white to yellow Solid
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Safety Information

HS Code 
2933399990
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ETHYL 2-(METHYLSULFONYL)PYRIMIDINE-5-CARBOXYLATE Usage And Synthesis

Synthesis

73781-88-1

148550-51-0

Step 2: Synthesis of ethyl 2-(methylsulfonyl)pyrimidine-5-carboxylate (121); Sulfide 120 (0.424 g, 2.14 mmol) was dissolved in dichloromethane (DCM, 9 mL), and a DCM (9 mL) solution of 3-chloroperoxybenzoic acid (mCPBA, 2.0 g) was slowly added. The reaction mixture was stirred at room temperature for 100 min. Upon completion of the reaction, the reaction was quenched with aqueous Na2S2O3, diluted with DCM and washed with saturated NaHCO3 solution. The organic phase was dried over anhydrous MgSO4, filtered and concentrated to give the target product 121 (0.374 g, 76% yield). [0726] MS: m/z 230.1 (calculated), 230.9 (measured).

References

[1] Synthetic Communications, 1993, vol. 23, # 6, p. 715 - 723
[2] Patent: WO2007/118137, 2007, A1. Location in patent: Page/Page column 105
[3] Chemical Biology and Drug Design, 2016, vol. 87, # 3, p. 472 - 477
[4] Patent: CN106279044, 2017, A. Location in patent: Paragraph 0026; 0030; 0070; 0071
[5] Patent: WO2012/117421, 2012, A1. Location in patent: Page/Page column 44

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