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Chemical Structure| 1072710-99-6 Chemical Structure| 1072710-99-6

Structure of 1072710-99-6

Chemical Structure| 1072710-99-6

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Product Details of [ 1072710-99-6 ]

CAS No. :1072710-99-6
Formula : C8H8ClN3O
M.W : 197.62
SMILES Code : O=C(C1CC1)NC2=NC=NC(Cl)=C2
MDL No. :MFCD20230069

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Application In Synthesis of [ 1072710-99-6 ]

* 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 [ 1072710-99-6 ]

[ 1072710-99-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1072710-99-6 ]
  • [ 74204-00-5 ]
  • [ 1529768-11-3 ]
YieldReaction ConditionsOperation in experiment
67.9% With caesium carbonate; In N,N-dimethyl-formamide; at 150℃; for 1.0h;Microwave irradiation; Add N-(6-chloropyrimidin-4-yl)cyclopropanecarboxamide (1 g, 5.07 mmol), <strong>[74204-00-5]3-bromo-5-methyl-phenol</strong> (950 mg, 5.07 mmol), Cs2CO3 (2.14 g, 6.60 mmol) and DMF (10 mL) to a microwave reaction vessel (25 mL). Heat the reaction under microwave conditions at 150° C. for 1 hr. Cool to room temperature, add water (50 mL), extract with EtOAc (100 mL*2), combine organic layers, dry over anhydrous Na2SO4. Concentration and purification by chromatography (silica gel, EtOAc:PE=1:3) afford the title compound (1.2 g, 67.9percent). MS: (M+1): 348.1.
1.2 g With caesium carbonate; In N,N-dimethyl-formamide; at 150℃; for 1.0h;Microwave irradiation; Add N-(6-chloropyrimidin-4-yl)cyclopropanecarboxamide (1 g, 5.07 mmol), <strong>[74204-00-5]3-bromo-5-methyl-phenol</strong> (950 mg, 5.07 mmol), Cs2C03 (2.14 g, 6.60 mmol) and DMF (10 mL) to a microwave reaction vessel (25 mL). Heat the reaction under microwave conditions at 150°C for 1 hr. Cool to room temperature, add water (50 mL), extract with EtOAc (100 mLx2), combine organic layers, dry over anhydrous Na2S04. Concentration and purification by chromatography (silica gel, EtOAc:PE=l:3) afford the title compound (1.2 g, 67.9percent). MS: (M+l): 348.1.
 

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