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Chemical Structure| 885271-93-2 Chemical Structure| 885271-93-2

Structure of 885271-93-2

Chemical Structure| 885271-93-2

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Product Details of [ 885271-93-2 ]

CAS No. :885271-93-2
Formula : C11H11FN2O2
M.W : 222.22
SMILES Code : O=C(OCC)CC1=NNC2=C1C=C(F)C=C2
English Name :Ethyl 2-(5-fluoro-1H-indazol-3-yl)acetate
MDL No. :MFCD06739128

Safety of [ 885271-93-2 ]

Application In Synthesis of [ 885271-93-2 ]

* 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 [ 885271-93-2 ]

[ 885271-93-2 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 395-81-3 ]
  • [ 885271-93-2 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1.1: formic acid / 0.5 h / 45 °C 1.2: 5 h / 45 - 95 °C 2.1: hydrazine hydrate; sodium hydroxide / 0.5 h / 80 °C 3.1: sulfuric acid / 16 h / Reflux
Multi-step reaction with 3 steps 1.1: formic acid / 0.5 h / 45 °C 1.2: 5 h / 70 - 95 °C 2.1: sodium hydroxide; hydrazine hydrate / 80 °C 3.1: sulfuric acid / 16 h / Reflux
  • 2
  • [ 682803-56-1 ]
  • [ 885271-93-2 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: hydrazine hydrate; sodium hydroxide / 0.5 h / 80 °C 2: sulfuric acid / 16 h / Reflux
Multi-step reaction with 2 steps 1: sodium hydroxide; hydrazine hydrate / 80 °C 2: sulfuric acid / 16 h / Reflux
  • 3
  • [ 885271-93-2 ]
  • [ 1437320-37-0 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: caesium carbonate / tetrahydrofuran / 0.5 h / 20 °C 1.2: 16 h 2.1: hydrogen; 10% Pd/C / methanol / 0.5 h
Multi-step reaction with 2 steps 1.1: caesium carbonate / tetrahydrofuran / 0.5 h / 20 °C 1.2: 16 h 2.1: hydrogen; 10% Pd/C / methanol / 0.5 h
  • 4
  • [ 885271-93-2 ]
  • [ 100-11-8 ]
  • [ 1437320-36-9 ]
YieldReaction ConditionsOperation in experiment
38.2% Stage #1: ethyl 2-(5-fluoro-1H-indazol-3-yl)acetate With caesium carbonate In tetrahydrofuran at 20℃; for 0.5h; Stage #2: 1-bromomethyl-4-nitro-benzene In tetrahydrofuran for 16h; 11.4 Preparation of ethyl 2-[5-fluoro-1-(4-nitrobenzyl)-1H-indazol-3-yl]acetate Ethyl 2-(5-fluoro-1H-indazol-3-yl) acetate (0.48 g, 2.16 mmol) was dissolved in anhydrous tetrahydrofuran (30 mL). Cesium carbonate (2.11 g, 6.48 mmol) was added, and stirred at room temperature for half an hour. Then p-nitro benzyl bromide (466 mg, 2.16 mmol) was added. After reacted for 16 hours, the solid was filtered. The filtrate was concentrated, chromatographed on a silica gel column (petroleum ether:ethyl acetate=2:1) to obtain a yellow solid 295 mg, at a yield of 38.2%.
38.2% Stage #1: ethyl 2-(5-fluoro-1H-indazol-3-yl)acetate With caesium carbonate In tetrahydrofuran at 20℃; for 0.5h; Stage #2: 1-bromomethyl-4-nitro-benzene In tetrahydrofuran for 16h; 11.4 4.
Preparation of ethyl 2-[5-fluoro-1-(4-nitrobenzyl)-1H-indazol-3-yl]acetate
Ethyl 2-(5-fluoro-1H-indazol-3-yl)acetate (0.48 g, 2.16 mmol) was dissolved in anhydrous tetrahydrofuran (30 mL). Cesium carbonate (2.11 g, 6.48 mmol) was added, and stirred at room temperature for half an hour. Then p-nitro benzyl bromide (466 mg, 2.16 mmol) was added. After reacted for 16 hours, the solid was filtered. The filtrate was concentrated, chromatographed on a silica gel column (petroleum ether:ethyl acetate=2:1) to obtain a yellow solid 295 mg, at a yield of 38.2%.
  • 5
  • [ 64-17-5 ]
  • [ 885271-22-7 ]
  • [ 885271-93-2 ]
YieldReaction ConditionsOperation in experiment
37.4% With sulfuric acid for 16h; Reflux; 11.3 Preparation of ethyl 2-(5-fluoro-1H-indazol-3-yl)acetate 2-(5-Fluoro-1H-indazol-3-yl)acetic acid (1.12 g, 5.77 mmol) was dissolved in anhydrous ethanol (50 mL) concentrated sulfuric acid (1.5 mL), and heated under reflux for 16 hours. After concentrated under reduce pressure to remove most of ethanol, water (20 mL) was added, and extracted with ethyl acetate. The organic phase was dried over anhydrous sodium sulfate, and concentrated to obtain the product 0.48 g, at a yield of 37.4%.
37.4% With sulfuric acid for 16h; Reflux; 11.3 3.
Preparation of ethyl 2-(5-fluoro-1H-indazol-3-yl)acetate
2-(5-Fluoro-1H-indazol-3-yl)acetic acid (1.12 g, 5.77 mmol) was dissolved in anhydrous ethanol (50 mL) concentrated sulfuric acid (1.5 mL), and heated under reflux for 16 hours. After concentrated under reduce pressure to remove most of ethanol, water (20 mL) was added, and extracted with ethyl acetate. The organic phase was dried over anhydrous sodium sulfate, and concentrated to obtain the product 0.48 g, at a yield of 37.4%.
  • 6
  • [ 885271-93-2 ]
  • [ 1437320-38-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: caesium carbonate / tetrahydrofuran / 0.5 h / 20 °C 1.2: 16 h 2.1: triethylamine / dichloromethane / 16 h / 20 °C / Cooling with ice
Multi-step reaction with 3 steps 1.1: caesium carbonate / tetrahydrofuran / 0.5 h / 20 °C 1.2: 16 h 2.1: hydrogen; 10% Pd/C / methanol / 0.5 h 3.1: triethylamine / dichloromethane / 16 h / 20 °C / Cooling with ice
  • 7
  • [ 885271-93-2 ]
  • [ 1437320-01-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1.1: caesium carbonate / tetrahydrofuran / 0.5 h / 20 °C 1.2: 16 h 2.1: triethylamine / dichloromethane / 16 h / 20 °C / Cooling with ice 3.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 3 h / 20 °C / Cooling with ice
Multi-step reaction with 4 steps 1.1: caesium carbonate / tetrahydrofuran / 0.5 h / 20 °C 1.2: 16 h 2.1: hydrogen; 10% Pd/C / methanol / 0.5 h 3.1: triethylamine / dichloromethane / 16 h / 20 °C / Cooling with ice 4.1: lithium hydroxide monohydrate / water; tetrahydrofuran / 3 h / 20 °C / Cooling with ice
 

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