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Chemical Structure| 202594-71-6 Chemical Structure| 202594-71-6

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Chemical Structure| 202594-71-6

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Product Details of [ 202594-71-6 ]

CAS No. :202594-71-6
Formula : C14H10ClNO
M.W : 243.69
SMILES Code : ClCC1=COC(C2=CC=C3C=CC=CC3=C2)=N1

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Application In Synthesis of [ 202594-71-6 ]

* 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 [ 202594-71-6 ]

[ 202594-71-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2243-82-5 ]
  • [ 534-07-6 ]
  • [ 202594-71-6 ]
YieldReaction ConditionsOperation in experiment
77% at 200℃; Procedure for the synthesis of chlorides 4A mixture of amide 2 (1 mmol) and 1,3- dichloroacetone (1.2 mmol) was warmed at T = 200 °C in homogeneous for 4-10 h. In case of tioamides 3 the mixture was dissolved in EtOH (50 mL) with the same stoichiometric values. Aqueous layer was extracted with CH2C12 (25 mL x 3) . The organic layers were combined and dried on Na2S04. Ossazoles and thiazoles derivatives were purified by column chromatography in the experimental conditions reported for each compound.
77% at 200℃; for 5h; General procedure: Intermediates aryloxazoles 9a?e were prepared condensing the corresponding amides 7a?e with 1,3-dichloroacetone (2 mmol) heating at 200 °C for 5 h. Arylthiazoles 10a?d were prepared condensing 8a?d (1 mmol) with 1,3-dichloroacetone (2 mmol) in EtOH (25 mL). After cooling at room temperature, water (10 mL) and AcOEt (10 mL) were added. The aqueous phase was extracted with AcOEt (3 × 50 mL) and the combined solution was dried over Na2SO4 and evaporated. The residue was purified on silica gel column chromatography in specific condition below reported for each compound.
77% at 200℃; General procedure: A mixture of amide 2 (1 mmol) and 1,3-dichloroacetone (1.2 mmol) was warmed at T=200° C. in homogeneous for 4-10 h. In case of tioamides 3 the mixture was dissolved in EtOH (50 mL) with the same stoichiometric values. Aqueous layer was extracted with CH2Cl2 (25 mL×3). The organic layers were combined and dried on Na2SO4. Ossazoles and thiazoles derivatives were purified by column chromatography in the experimental conditions reported for each compound.
68% Reference Example 43 In substantially the same manner as in Reference Example 31, 2-naphthalenecarboxamide was allowed to react with 1,3-dichloroacetone to give 4-chloromethyl-2-(2-naphthyl)oxazole. The yield was 68percent. Recrystallization from ethyl acetate-hexane gave colorless prisms, mp 116-117° C.

 

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