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Chemical Structure| 169905-10-6 Chemical Structure| 169905-10-6

Structure of 169905-10-6

Chemical Structure| 169905-10-6

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Product Details of [ 169905-10-6 ]

CAS No. :169905-10-6
Formula : C8H10ClNO2
M.W : 187.62
SMILES Code : COC1=C(OC)C(CCl)=NC=C1
MDL No. :MFCD03265307

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Application In Synthesis of [ 169905-10-6 ]

* 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 [ 169905-10-6 ]

[ 169905-10-6 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 72830-08-1 ]
  • [ 169905-10-6 ]
YieldReaction ConditionsOperation in experiment
88% With thionyl chloride; In dichloromethane; EXAMPLE I 3 Preparation of 3,4-dimethoxy-2-chloromethylpyridine 3,4-Dimethoxy-2-hydroxymethylpyridine (0.34 g, 0.002 mol) was dissolved in CH2 Cl2 (8 ml). SOCl2 (0.27 g, 0.00227 mol) in CH2 Cl2 (2 ml) was added under stirring at room temperature. After 10 min the mixture was neutralized with NaHCO3 (5 ml). The phases were separated, the CH2 Cl2 phase was washed with NaCl-solution, dried over Na2 SO4 and evaporated giving the desired product (0.61 g, 88%).
88% With thionyl chloride; In dichloromethane; Example I 1. Preparation of 3,4-dimethoxy-2-chloromethylpyridine. 3,4-Dimethoxy-2-hydroxymethylpyridine (0.34 g, 0.002 mol) was dissolved in CH2 Cl2 (8 ml). SOCl2 (0.27 g, 0.00227 mol) in CH2 Cl2 (2 ml) was added under stirring at room temperature. After 10 min the mixture was neutralized with NaHCO3 (5 ml). The phases were separated, the CH2 Cl2 phase was washed with NaCl-solution, dried over Na2 SO4 and evaporated giving the desired product (0.61 g, 88%).
  • 2
  • [ 169905-10-6 ]
  • [ 97963-62-7 ]
  • [ 102625-64-9 ]
YieldReaction ConditionsOperation in experiment
87.8% With sodium hydroxide; In water; isopropyl alcohol; at 20℃; for 3h; [EXAMPLE 1]Preparation of 5-difluoromethoxy-2-(3,4-dimethoxy-benzylsulfanyl)-lH- benzimidazole 92OmL of isopropanol, 92.1g of 5-difluoromethoxy-2- mercaptobenzimidazole and 95.8g of 2-chloromethyl-3,4-dimethoxypyridine were introduced into a reactor. After adding a sodium hydroxide solution (containing 20.5g of sodium hydroxide in 92OmL of purified water) dropwise to the above mixture, this reaction mixture was stirred at room temperature for 2 hours. Introducing 92OmL of purified water to the mixture and stirring the same for 1 hour, the resultant solid material was subjected to filtration and vacuum drying, thus yielding a final product.Amount of final product: 137.4g (yield: 87.8%)MP: 94 C
  • 3
  • [ 169905-10-6 ]
  • [ 97963-62-7 ]
  • pantoprazole [ No CAS ]
 

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