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Chemical Structure| 1245914-05-9 Chemical Structure| 1245914-05-9

Structure of 1245914-05-9

Chemical Structure| 1245914-05-9

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Synonyms: 1,1-Dimethylethyl 4-(5-amino-3-pyridinyl)-1-piperazinecarboxylate

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Product Details of [ 1245914-05-9 ]

CAS No. :1245914-05-9
Formula : C14H22N4O2
M.W : 278.35
SMILES Code : O=C(N1CCN(C2=CC(N)=CN=C2)CC1)OC(C)(C)C
Synonyms :
1,1-Dimethylethyl 4-(5-amino-3-pyridinyl)-1-piperazinecarboxylate
English Name :tert-Butyl 4-(5-aminopyridin-3-yl)piperazine-1-carboxylate

Safety of [ 1245914-05-9 ]

Application In Synthesis of [ 1245914-05-9 ]

* 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 [ 1245914-05-9 ]

[ 1245914-05-9 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 2252258-77-6 ]
  • [ 1245914-05-9 ]
  • [ 2252258-82-3 ]
YieldReaction ConditionsOperation in experiment
35% With tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene In 1,4-dioxane at 80℃; Inert atmosphere; 1 Tert-butyl 4-(5-((3-(2-chlorophenyl)-l-methyl-2-oxo-l,2-dihydro-l,6- naphthyridin-7 -yl) amino)pyridin- 3 -yl)piperazine- 1 -c arboxylate (71) To a pre-heated round bottom flask, 56 (42 mg, 0.13 mmol), 70 (39 mg, 0.13 mmol), Pd2(dba)3 (13 mg, 0.013 mmol), Xantphos (16 mg, 0.027 mmol) and caesium carbonate (90 mg, 0.27 mmol) was added and flushed with argon for 10 min. Dioxane (3 mL) was added to the mixture and flushed again for 5 min and then heated overnight at 80 °C. The reaction mixture was then partitioned between ethyl acetate and water, dried over anhydrous Na2S04, filtered, concentrated and purified by column chromatography using silica gel (2.5 % MeOH/DCM) to give 71 (26 mg, 35%) as light brown solid.
35% With tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene In 1,4-dioxane at 80℃; Tert-butyl 4-(5-((3-(2-chlorophenyl)-1-methyl-2-oxo-1-2-dihydro-1-6- naphthyridin-7-yl)amino)pyridin-3-yl)piperazine-1-carboxylate (71): To a pre-heated round bottom flask, 56 (42 mg, 0.13 mmol), 70 (39 mg, 0.13 mmol), Pd2(dba)3 (13 mg, 0.013 mmol), Xantphos (16 mg, 0.027 mmol) and caesium carbonate (90 mg, 0.27 mmol) was added and flushed with argon for 10 min. Dioxane (3 mL) was added to the mixture and flushed again for 5 min and then heated overnight at 80 °C. The reaction mixture was then partitioned between ethyl acetate and water, dried over anhydrous Na2SO4, filtered, concentrated and purified by column chromatography using silica gel (2.5 % MeOH/DCM) to give 71 (26 mg, 35%) as light brown solid.
  • 2
  • [ 2252258-77-6 ]
  • [ 1245914-05-9 ]
  • [ 2252258-43-6 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 80 °C / Inert atmosphere 2: trifluoroacetic acid / dichloromethane / 2 h / 20 °C / Inert atmosphere
Multi-step reaction with 2 steps 1: tris-(dibenzylideneacetone)dipalladium(0); 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; caesium carbonate / 1,4-dioxane / 80 °C 2: trifluoroacetic acid / dichloromethane / 2 h / 20 °C
  • 3
  • [ 2252258-81-2 ]
  • [ 1245914-05-9 ]
YieldReaction ConditionsOperation in experiment
97% With 10% Pd/C; hydrogen In methanol at 20℃; Tert-butyl 4-(5-aminopyridin-3-yl)piperazine-1-carboxylate (70): To a solution of 69 (250 mg, 0.81 mmol) in CH3OH (15 mL) was added 10% Pd/C (50 mg) and the reaction was stirred at room temperature in (g) (1 atm) for 4 h. The reaction mixture was then filtered through celite and concentrated to afford 70 (220 mg, 97%) as brown solid which was used in next step without purification.
96% With 10% Pd/C; hydrogen In methanol at 20℃; 1 Tert-butyl 4-(5-aminopyridin-3-yl)piperazine-l-carboxylate (70): To a solution of 69 (250 mg, 0.81 mmol) in CH3OH (15 mL) was added 10% Pd/C (50 mg) and the reaction was stirred at room temperature in (g) (1 atm) for 4 h. The reaction mixture was then filtered through celite and concentrated to afford 70 (220 mg, 97%) as brown solid which was used in next step without purification.
  • 4
  • [ 15862-30-3 ]
  • [ 1245914-05-9 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: tris-(dibenzylideneacetone)dipalladium(0); Xantphos / 1,4-dioxane / 24 h / Reflux; Inert atmosphere 2: 10% Pd/C; hydrogen / methanol / 20 °C / 760.05 Torr
Multi-step reaction with 2 steps 1: tris-(dibenzylideneacetone)dipalladium(0); Xantphos; potassium carbonate / 24 h / Reflux 2: 10% Pd/C; hydrogen / methanol / 20 °C / 760.05 Torr
  • 5
  • [ 57260-71-6 ]
  • [ 1245914-05-9 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: tris-(dibenzylideneacetone)dipalladium(0); Xantphos / 1,4-dioxane / 24 h / Reflux; Inert atmosphere 2: 10% Pd/C; hydrogen / methanol / 20 °C / 760.05 Torr
Multi-step reaction with 2 steps 1: tris-(dibenzylideneacetone)dipalladium(0); Xantphos; potassium carbonate / 24 h / Reflux 2: 10% Pd/C; hydrogen / methanol / 20 °C / 760.05 Torr
 

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