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Chemical Structure| 101667-98-5 Chemical Structure| 101667-98-5

Structure of 101667-98-5

Chemical Structure| 101667-98-5

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Product Details of [ 101667-98-5 ]

CAS No. :101667-98-5
Formula : C10H9ClN2O2S
M.W : 256.71
SMILES Code : CCOC(=O)C1=C(C)C2=C(S1)N=CN=C2Cl
MDL No. :MFCD01097096
InChI Key :FIIBPXMYXHXUPI-UHFFFAOYSA-N
Pubchem ID :2103964

Safety of [ 101667-98-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H319
Precautionary Statements:P305+P351+P338

Application In Synthesis of [ 101667-98-5 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 101667-98-5 ]

[ 101667-98-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 623-51-8 ]
  • [ 60025-06-1 ]
  • [ 101667-98-5 ]
YieldReaction ConditionsOperation in experiment
41% With potassium carbonate; In N,N-dimethyl-formamide; at 20℃;Inert atmosphere; To a solution of <strong>[60025-06-1]1-(4,6-dichloropyrimidin-5-yl)ethan-1-one</strong> (1.00 g, 5.24 mmol) in DMF (30 ml.) was added ethyl 2-mercaptoacetate (755 mg, 6.29 mmol) and K2CO3 (2.17 g, 15.7 mmol) and the mixture was stirred at room temperature under nitrogen overnight. The mixture was poured into water and extracted with EtOAc (100 ml. x 3). The combined organic extracts were washed with brine (100 ml_), dried over Na2S04, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography (Pet. Ether/EtOAc = 200:1 to 40:1 ) to give the title compound (276 mg, 41%) as a white solid. LCMS-F: rt 3.12 min; m/z 257.0 [M+H]+.
 

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