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Chemical Structure| 690257-76-2 Chemical Structure| 690257-76-2

Structure of 690257-76-2

Chemical Structure| 690257-76-2

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Product Details of [ 690257-76-2 ]

CAS No. :690257-76-2
Formula : C3H6FN
M.W : 75.08
SMILES Code : FC1CNC1
MDL No. :MFCD09756543
InChI Key :WQYAZBFZFIUIPL-UHFFFAOYSA-N
Pubchem ID :3603542

Safety of [ 690257-76-2 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H225-H314
Precautionary Statements:P210-P280-P305+P351+P338-P310
Class:3(8)
UN#:2924
Packing Group:

Application In Synthesis of [ 690257-76-2 ]

* 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 [ 690257-76-2 ]

[ 690257-76-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 690257-76-2 ]
  • [ 22280-60-0 ]
  • [ 1435954-08-7 ]
YieldReaction ConditionsOperation in experiment
92% With caesium carbonate; In N,N-dimethyl-formamide; at 80℃; for 2h; General procedure: To a solution of <strong>[22280-60-0]6-chloro-2-methyl-3-nitropyridine</strong> (0.5 g, 2.9 mmol) in DMF (5 mL) was added Cs2C03 (1.9 g, 5.8 mmol) followed 3-fluoroazetidine (0.64 g, 5.8 mmol) and the reaction mixture was heated for 2 h at 80°C. The reaction mixture was then diluted with EtOAc and the organic layer was washed with saturated aqueous sodium bicarbonate solution. The organic layer was then dried over sodium sulphate and concentrated. The crude material obtained was purified by column chromatography (silica: 100-200 mesh, MeOF DCM 2-3percent) to afford the title compound (0.6 g, 92percent). LCMS (ES+) 21 1.95 (M+H)+, RT 2.33 minutes (method 1).
92% With caesium carbonate; In N,N-dimethyl-formamide; at 80℃; for 2h; Intermediate 49 6-(3-Fluoroazetidin-1-yl)-2-methyl-3-nitropyridine [0269] To a solution of <strong>[22280-60-0]6-chloro-2-methyl-3-nitropyridine</strong> (0.5 g, 2.9 mmol) in DMF (5 mL) was added Cs2CO3 (1.9 g, 5.8 mmol) followed 3-fluoroazetidine (0.64 g, 5.8 mmol) and the reaction mixture was heated for 2 h at 80° C. The reaction mixture was then diluted with EtOAc and the organic layer was washed with saturated aqueous sodium bicarbonate solution. The organic layer was then dried over sodium sulphate and concentrated. The crude material obtained was purified by column chromatography (silica: 100-200 mesh, MeOH: DCM 2-3percent) to afford the title compound (0.6 g, 92percent). LCMS (ES+) 211.95 (M+H)+, RT 2.33 minutes (method 1).
 

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