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Chemical Structure| 1160066-14-7 Chemical Structure| 1160066-14-7

Structure of 1160066-14-7

Chemical Structure| 1160066-14-7

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Product Details of [ 1160066-14-7 ]

CAS No. :1160066-14-7
Formula : C7H7Cl2N3O
M.W : 220.06
SMILES Code : O=C(N(C)C)C1C(Cl)=NC(Cl)=NC=1

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Application In Synthesis of [ 1160066-14-7 ]

* 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 [ 1160066-14-7 ]

[ 1160066-14-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 124-40-3 ]
  • [ 2972-52-3 ]
  • [ 1160066-14-7 ]
YieldReaction ConditionsOperation in experiment
100% With triethylamine; In dichloromethane; at 0 - 20℃; Example 59: Synthesis of 2,4-dichloro-pyrimidine-5-carboxylic acid dimethylamide; To a solution of 2,4-dichloro-pyrimidine-5-carbonyl chloride (197.7 mg, 0.94 mmol) in CH2CI2 (9.4 mL) at RT is added Me2NH (2.0 /W THF solution, 390 μl_, 0.78 mmol) and Et3N (108.6 μl_, 0.78 mmol) at 0 0C. The reaction mixture is stirred overnight at RT. After adding water, the mixture is extracted with CH2CI2. The organic layer is dried and concentration under reduce pressure give 2,4-dichloro-pyrimidine-5-carboxylic acid dimethylamide (272.5 mg, quant). ESI-MS m/z: 221 [M+1]+, Retantion time 1.94 min (condition B).
77% With triethylamine; In dichloromethane; at 0 - 25℃; for 3h; <strong>[2972-52-3]2,4-dichloropyrimidine-5-carbonyl chloride</strong> (1.0 eq.) Was added to CH2Cl2 (0.1 M) to dissolve, dimethylamine (0.8 eq.) And TEA (0.8 eq.) Were added at 0 oC, and then at room temperature. Was reacted for 3 hours. Water was poured into the reaction mixture, followed by extraction with CH2Cl2. (X3) The collected organic layer was removed with MgSO4. After filtration, it was concentrated and the compound was purified by MPLC (EtOAc: Hex). After concentration, the desired compound was obtained as a light yellow liquid. (Yield: 77%)
 

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