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Chemical Structure| 1019384-02-1 Chemical Structure| 1019384-02-1

Structure of 1019384-02-1

Chemical Structure| 1019384-02-1

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Product Details of [ 1019384-02-1 ]

CAS No. :1019384-02-1
Formula : C15H11ClN2S
M.W : 286.78
SMILES Code : ClC1=C(C(C2=CC=CC=C2)=CS3)C3=NC(C4CC4)=N1
MDL No. :MFCD12531439

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Application In Synthesis of [ 1019384-02-1 ]

* 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 [ 1019384-02-1 ]

[ 1019384-02-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1019384-02-1 ]
  • [ 25602-68-0 ]
  • [ 1437774-77-0 ]
YieldReaction ConditionsOperation in experiment
0.15 g With triethylamine; In ethanol; at 20 - 140℃;Microwave irradiation; ) 8-(2-cyclopropyl-5-phenyl-thieno[2,3-d]pyrimidin-4-yl)-8-azabicyclo[3.2.1] octan- 3 -oneA mixture of 4-chloro-2-cyclopropyl-5-phenyl-thieno[2,3-d]pyrimidine (0.30 g, 1.05 mmol, ex Enamine), <strong>[25602-68-0]nortropinone hydrochloride</strong> (0.25 g, 1.57 mmol) and triethylamine (0.44 mL, 3.14 mmol) in ethanol (4 mL) was heated to 140 °C for 30 min in a microwave. Heating was repeated. Further portions of triethylamine (0.44 mL, 3.14 mmol) and <strong>[25602-68-0]nortropinone hydrochloride</strong> (0.25 g, 1.57 mmol) were added and the mixture was stirred at room temperature for 3 nights. It was diluted with ethyl acetate (20 mL) and water (20 mL). The layers were separated and the aqueous was extracted with ethyl acetate (2 x 20 mL). The combined organic layers were washed with brine (1 x 20 mL), dried (magnesium sulfate, filtered and evaporated to give a brown oil (512 mg). This was purified by silica chromatography (10 g cartridge; eluent petroleum ether 40-60 / ethyl acetate 0 to 100percent; all output collected) to give 8-(2-cyclopropyl-5-phenyl-thieno[2,3-d]pyrimidin-4-yl)-8- azabicyclo[3.2.1]octan-3-oneas a yellow solid (0.15 g). m/z [M+H]+ 376.0. Retention time 4.98 min (LCMS method +ve 6 min).
0.15 g With triethylamine; In ethanol; at 20 - 140℃;Microwave irradiation; i) 8-(2-cyclopropyl-5-phenyl-thieno[2,3-d]pyrimidin-4-yl)-8-azabicyclo[3.2.1]octan-3-one A mixture of 4-chloro-2-cyclopropyl-5-phenyl-thieno[2,3-d]pyrimidine (0.30 g, 1.05 mmol, ex Enamine), <strong>[25602-68-0]nortropinone hydrochloride</strong> (0.25 g, 1.57 mmol) and triethylamine (0.44 mL, 3.14 mmol) in ethanol (4 mL) was heated to 140° C. for 30 min in a microwave. Heating was repeated. Further portions of triethylamine (0.44 mL, 3.14 mmol) and <strong>[25602-68-0]nortropinone hydrochloride</strong> (0.25 g, 1.57 mmol) were added and the mixture was stirred at room temperature for 3 nights. It was diluted with ethyl acetate (20 mL) and water (20 mL). The layers were separated and the aqueous was extracted with ethyl acetate (2*20 mL). The combined organic layers were washed with brine (1*20 mL), dried (magnesium sulfate, filtered and evaporated to give a brown oil (512 mg). This was purified by silica chromatography (10 g cartridge; eluent petroleum ether 40-60/ethyl acetate 0 to 100percent; all output collected) to give 8-(2-cyclopropyl-5-phenyl-thieno[2,3-d]pyrimidin-4-yl)-8-azabicyclo[3.2.1]octan-3-oneas a yellow solid (0.15 g). m/z [M+H]+ 376.0. Retention time 4.98 min (LCMS method +ve 6 min).
  • 2
  • [ 1019384-02-1 ]
  • [ 25602-68-0 ]
  • [ 1437773-60-8 ]
 

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