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Chemical Structure| 947179-19-3 Chemical Structure| 947179-19-3

Structure of 947179-19-3

Chemical Structure| 947179-19-3

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Product Details of [ 947179-19-3 ]

CAS No. :947179-19-3
Formula : C9H12F2N2O2S
M.W : 250.27
SMILES Code : CC(C)(C)OC(=O)NC1=NC(=CS1)C(F)F
MDL No. :MFCD18833784
InChI Key :YQYPCZYHSSWKET-UHFFFAOYSA-N
Pubchem ID :45117843

Safety of [ 947179-19-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 947179-19-3 ]

* 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 [ 947179-19-3 ]

[ 947179-19-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 494769-34-5 ]
  • [ 947179-19-3 ]
YieldReaction ConditionsOperation in experiment
60% Step 1: (4-Difluoromethylthiazol-2-yl)-carbamic acid tert-butyl ester To a solution of 1.25 g (5.5 mmol) <strong>[494769-34-5](4-formyl-thiazol-2-yl)-carbamic acid tert-butyl ester</strong> (CAS: [494769-34-5]) in 30 ml of dry methylene chloride were added 2.15 ml (16.4 mmol) diethylaminosulfur trifluoride (DAST). The mixture was stirred at room temperature for 16 hours. The reaction mixture was quenched with sat. NaHCO3- solution and extracted with water and methylene chloride. The combined organic extracts were dried with sodium sulfate, filtered and evaporated. The crude product was purified by flash chromatography on silica gel (heptane/ethyl acetate 4:1). The desired compound was obtained as a yellow solid (810 mg, 60%), MS: m/e=251.2 (M+H)+.
5.8 g With diethylamino-sulfur trifluoride; In ethanol; dichloromethane; at 20℃; To a solution of Compound AH (7.0 g, 31 mmol) in DCM (200 mL) and EtOH (100 mL) was added DAST (7.4 g, 46.05 mmol). The reaction mixture was stirred at room temperature overnight. The mixture was poured into water and diluted with DCM (200 mL), and then washed with water (100 mL), sat. NaHC03 (100 mL). The organic layer was dried and concentrated to afford light yellow oil. The residue was purified by column chromatography in silica gel (PE: EA =30: 1) to give the Compound AI (5.8 g) as a light yellow solid.
5.8 g With diethylamino-sulfur trifluoride; In ethanol; dichloromethane; at 20℃; To a solution of CompoundAR (7.0 g, 31 mmol) inDCM (200 mL) and EtOR (100 mL) was added DAST (7.4 g,46.05 mmol). The reaction mixture was stirred at room temSperature overnight. The mixture was poured into water anddiluted with DCM (200 mL), and then washed with water(100 mL), sat. NaHCO3 (100 mL). The organic layer wasdried and concentrated to afford light yellow oil. The residuewas purified by column chromatography in silica gel (PE:EA=30: 1) to give the Compound Al (5.8 g) as a light yellow
 

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