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Chemical Structure| 1260384-38-0 Chemical Structure| 1260384-38-0

Structure of 1260384-38-0

Chemical Structure| 1260384-38-0

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Product Details of [ 1260384-38-0 ]

CAS No. :1260384-38-0
Formula : C7H4ClIN2
M.W : 278.48
SMILES Code : IC1=CN=C(Cl)C2=C1C=CN2
MDL No. :MFCD18381044

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Application In Synthesis of [ 1260384-38-0 ]

* 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 [ 1260384-38-0 ]

[ 1260384-38-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1826-67-1 ]
  • [ 426463-05-0 ]
  • [ 1260384-38-0 ]
YieldReaction ConditionsOperation in experiment
9% With O-phenyl phosphorodichloridate; In 2-methyltetrahydrofuran; at -70℃; for 1.25h;Inert atmosphere; [0659] To a solution of vinyl magnesium bromide (66 mL, 66 mmol, 3.4 eq, 1.0 M solution in 2-methyl tetrahydrofuran) at -70 C. under nitrogen was added a solution of XIII-3 (5.5 g, 19.3 mmol, 1 eq.) in 120 mL of dry tetrahydrofuran, dropwise over 45 min. After 30 min at -70 C. TLC analysis (PE:EA=3:1) showed the starting material was consumed completely. The reaction was quenched with saturated ammonium chloride (50 mL). The mixture was extracted with ethyl acetate (150 mL×3). The combined organic layers was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated to give a brown oil. It was purified by flash chromatography on silica gel with petroleum ether/EtOAc (5:1?2:1) to give XIII-4 (0.5 g, 9% yield). MS (ESI) m/z (M+H)+ 278.8.
9% In tetrahydrofuran; 2-methyltetrahydrofuran; at -70℃; for 1.25h;Inert atmosphere; To a solution of vinyl magnesium bromide (66 mL, 66 mmol, 3.4 eq, 1.0 M solution in 2-methyl tetrahydrofuran) at -70C under nitrogen was added a solution of XIII-3 (5.5 g,19.3 mmol, 1 eq.) in 120 mL of dry tetrahydrofuran, dropwise over 45 mm. After 30 mm at -70C TLC analysis (PE:EA=3: 1) showed the starting material was consumed completely. The reaction was quenched with saturated ammonium chloride (50 mL). The mixture was extracted with ethyl acetate (150 mLx3). The combined organic layers was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated to give a brown oil. It was purified by flash chromatography on silica gel with petroleum ether/EtOAc (5: 1-*2: 1) to give X-4 (0.5 g, 9% yield). MS (ES) m/z (M+H) 278.8.
 

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