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Chemical Structure| 914204-71-0 Chemical Structure| 914204-71-0

Structure of 914204-71-0

Chemical Structure| 914204-71-0

Ethyl 6-(4-fluorophenyl)-3-methylimidazo[2,1-b]thiazole-2-carboxylate

CAS No.: 914204-71-0

4.5 *For Research Use Only !

Cat. No.: A553379 Purity: 97%

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Product Details of [ 914204-71-0 ]

CAS No. :914204-71-0
Formula : C15H13FN2O2S
M.W : 304.34
SMILES Code : O=C(C1=C(C)N2C(S1)=NC(C3=CC=C(F)C=C3)=C2)OCC
MDL No. :MFCD08815639

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Application In Synthesis of [ 914204-71-0 ]

* 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 [ 914204-71-0 ]

[ 914204-71-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 7210-76-6 ]
  • [ 403-29-2 ]
  • [ 914204-71-0 ]
YieldReaction ConditionsOperation in experiment
91% With polyethylene glycol (PEG-400); In water; for 0.116667h;Microwave irradiation; Green chemistry; To stirred solution of polyethylene glycol (PEG-400) (2 mL) in water (2 mL) were added 1-(2-amino-4-methylthiazol-5-yl)ethanone (2 mmol)/ethyl 2-amino-4-methylthiazole-5-carboxylate (2 mmol) and α-bromo aralkyl ketones (phenacyl bromides) (2 mmol), and the mixture was heated at 90 C or subject to microwave irradiation at 300 W, until reaction completion as indicated by TLC. After reaction completion, the reaction mixture was cooled at room temperature, and the solid product formed was collected by filtration, washed with water, and recrystallized from ethanol to give pure product. The recovered PEG with water was reused for five further cycles.
32% In ethanol; at 95℃; for 14h; 2-Bromo-1-(4-fluoro-phenyl)-ethanone (200 mg, 0.92 mmol) and 2-amino-4-methyl- thiazole-5-carboxylic acid ethyl ester (186.2 mg, 0.92 mmol) were heated in 5 ml of ethanol at 95 0C for 5 hours. After addition of 80 mg of 2-bromo-1-(4-fluoro-phenyl)- ethanone and further heating for 9 hours at 95C the mixture was evaporated. Addition of potassium hydrogensulfate solution, extraction with ethyl acetate and purification by preparative HPLC (RP18, acetonitrile/water 0.1 % TFA) yielded 81 mg (32%) of the desired product. MS (mass spectrum): M+H+ = 305.07.
 

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