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Chemical Structure| 675148-38-6 Chemical Structure| 675148-38-6

Structure of 675148-38-6

Chemical Structure| 675148-38-6

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Product Details of [ 675148-38-6 ]

CAS No. :675148-38-6
Formula : C13H12ClNO3
M.W : 265.69
SMILES Code : O=C(OC)C1=CC=C(C2=NC(CCl)=C(C)O2)C=C1
MDL No. :MFCD09758988

Safety of [ 675148-38-6 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H314
Precautionary Statements:P264-P270-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P403+P233-P501
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 675148-38-6 ]

* 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 [ 675148-38-6 ]

[ 675148-38-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 675148-38-6 ]
  • [ 134464-79-2 ]
  • tert-butyl 4-((2-(4-(methoxycarbonyl)phenyl)-5-methyloxazol-4-yl)methylthio)piperidine-1-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
920 mg With potassium carbonate; In N,N-dimethyl-formamide; at 50℃; A mixture of the crude ie/t-butyl 4-mercaptopiperidine-l-carboxylate (2.34 g, 10.78 mmol, 1.20 equiv), methyl 4-(4-(chloromethyl)-5-methyloxazol-2-yl)benzoate (2.33 g, 8.79 mmol, 1.00 equiv) and potassium carbonate (1.74 g, 12.39 mmol, 1.50 equiv) in N,N-dimethylformamide (23.4 mL) was stirred overnight in a 100-mL round- bottom flask at 50C. The reaction mixture was then quenched by the addition of 30 mL of water. The resulting solution was extracted with 3x30 mL of ethyl acetate and the organic layers combined. The organic layer was washed with 2x40 mL of brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was eluted with ethyl acetate/petroleum ether (1 :30-1 :5) on a silica gel column to give 920 mg (23%) of ie/t-butyl 4-((2-(4-(methoxycarbonyl)phenyl)-5-methyloxazol-4- yl)methylthio)piperidine- l-carboxylate as a yellow solid. LC-MS: (ES, m/z): 447 [M+H]+, 347, 271, 146, 105.
920 mg With potassium carbonate; In N,N-dimethyl-formamide; A mixture of the crude <strong>[134464-79-2]tert-butyl 4-mercaptopiperidine-1-carboxylate</strong> (2.34 g, 10.78 mmol, 1.20 equiv), methyl 4-(4-(chloromethyl)-5-methyloxazol-2-yl)benzoate (2.33 g, 8.79 mmol, 1.00 equiv) and potassium carbonate (1.74 g, 12.39 mmol, 1.50 equiv) in N,N-dimethylformamide (23.4 mL) was stirred overnight in a 100-mL round-bottom flask at 50 C. The reaction mixture was then quenched by the addition of 30 mL of water. The resulting solution was extracted with 3×30 mL of ethyl acetate and the organic layers combined. The organic layer was washed with 2×40 mL of brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was eluted with ethyl acetate/petroleum ether (1:30-1:5) on a silica gel column to give 920 mg (23%) of tert-butyl 4-((2-(4-(methoxycarbonyl)phenyl)-5-methyloxazol-4-yl)methylthio)piperidine-1-carboxylate as a yellow solid. LC-MS: (ES, m/z): 447 [M+H]+, 347, 271, 146, 105.
 

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