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Chemical Structure| 1246632-85-8 Chemical Structure| 1246632-85-8

Structure of 1246632-85-8

Chemical Structure| 1246632-85-8

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Product Details of [ 1246632-85-8 ]

CAS No. :1246632-85-8
Formula : C7H6ClFN2O2
M.W : 204.59
SMILES Code : CCOC(C1=NC(Cl)=NC=C1F)=O
MDL No. :MFCD30742681
InChI Key :YGHPIVLSUXRHNF-UHFFFAOYSA-N
Pubchem ID :117902240

Safety of [ 1246632-85-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 1246632-85-8 ]

* 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 [ 1246632-85-8 ]

[ 1246632-85-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 88675-24-5 ]
  • [ 1246632-85-8 ]
  • ethyl 2-chloro-5-(tetrahydrofuran-3-ylamino)pyrimidine-4-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
77% With caesium carbonate; N-ethyl-N,N-diisopropylamine; In dimethyl sulfoxide; at 90℃;Inert atmosphere; General procedure: To a solution of nitrogen-containing nucleophile (1 eq.) and cesium carbonate (3.0 eq.) in N,N-dimethylformamide (2 mL/mmol) was added 2-haloheterocycle (1.1 eq.). Thereaction was heated to 100° C. and stirred at this temperature for 2 hours. Thereaction was then cooled to room temperature and acidified to pH=1 with 10percentaqueous HCl solution if product contains a carboxylic acid, or diluted withwater if neutral. The solution was extracted with twice with dichloromethane.The organic layers were combined, dried with sodium sulfate and concentratedunder vacuum. The crude material was either used directly in subsequentreactions or purified by flash chromatography.
77% With N-ethyl-N,N-diisopropylamine; In dimethyl sulfoxide; at 90℃; General procedure: Similar to as described in General Procedure A, ethyl 2-chloro-5-fluoropyrimidine-4-carboxylatewas reacted with oxolan-3-amine to give the title compound (535 mg, 77percent) as a yellow solid.LC-MS (ES, mlz): 272 [M+H].To a solution of nitrogen-containing nucleophile (1 eq.) and cesium carbonate (3.0 eq.) in N,N-dimethylformamide (2 mL/mmol) was added 2-haloheterocycle (1.1 eq.). The reaction washeated to 100 °C and stirred at this temperature for 2 hours. The reaction was then cooled to room temperature and acidified to pH = 1 with 10 percent aqueous HCl solution if product contains a carboxylic acid, or diluted with water if neutral. The solution was extracted with twice with dichloromethane. The organic layers were combined, dried with sodium sulfate and concentrated under vacuum. The crude material was either used directly in subsequent reactions or purified byflash chromatography
 

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