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Chemical Structure| 1252662-43-3 Chemical Structure| 1252662-43-3

Structure of 1252662-43-3

Chemical Structure| 1252662-43-3

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Product Details of [ 1252662-43-3 ]

CAS No. :1252662-43-3
Formula : C4H5BN2O3
M.W : 139.91
SMILES Code : O=C1C(B(O)O)=CC=NN1

Safety of [ 1252662-43-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 1252662-43-3 ]

* 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 [ 1252662-43-3 ]

[ 1252662-43-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1677-79-8 ]
  • [ 1252662-43-3 ]
YieldReaction ConditionsOperation in experiment
A microwave vial was charged with 52b (0.400 g, 3 mmol), delta-(pinacolato)diboron (0.934 g, 4 mmol), dicyclohexyl[2',4',6'-tr°(l-methylethyl)[l,l'-biphenyl]-2-yl]-phosphine (X- Phos, 0.058 g, 0.12 mmol), Pd2(dba)3 (0.056 g, 0.061 mmol) and KOAc (0.902 g, 9 mmol) and the flask was evacuated and back-filled with Ar and sealed. Dioxane (6 mL) was added and the reaction heated at 110 0C overnight. The reaction mixture was cooled to RT and extracted with EtOAc (120 mL). The organic extract was washed sequentially with H2O (10 mL) and brine (10 mL), dried (Na2SO4), filtered and evaporated. The crude product was triturated with Et2O to afford 0.217 g of 54.
  • 2
  • [ 1677-79-8 ]
  • [ 73183-34-3 ]
  • [ 1252662-43-3 ]
YieldReaction ConditionsOperation in experiment
With potassium acetate;bis(dibenzylideneacetone)-palladium(0); XPhos; In 1,4-dioxane; at 110.0℃;Inert atmosphere; sealed tube; step b-; A microwave vial was charged with 75 (0.400 g, 3 mmol), bis-(pinacolato)diboron (0.934 g, 4 mmol), dicyclohexyl[2',4',6'-tris(1-methylethyl)[1,1'-biphenyl]-2-yl]-phosphine (X-Phos, 0.058 g, 0.12 mmol), Pd2(dba)3 (0.056 g, 0.061 mmol) and KOAc (0.902 g, 9 mmol) and the flask was evacuated and back-filled with Ar and sealed. Dioxane (6 mL) was added and the reaction heated at 110 C. overnight. The reaction mixture was cooled to RT and extracted with EtOAc (120 mL). The organic extract was washed sequentially with H2O (10 mL) and brine (10 mL), dried (Na2SO4), filtered and evaporated. The crude product was triturated with Et2O to afford 0.217 g of 78.
With potassium acetate; XPhos;tris-(dibenzylideneacetone)dipalladium(0); In 1,4-dioxane; at 110.0℃;Inert atmosphere; A microwave vial was charged with 74 (0.400 g, 3 mmol), bis-(pinacolato)diboron (0.934 g, 4 mmol), dicyclohexyl[2',4',6'-tris(1-methylethyl)[1,1'-biphenyl]-2-yl]-phosphine (X-Phos, 0.058 g, 0.12 mmol), Pd2(dba)3 (0.056 g, 0.061 mmol) and KOAc (0.902 g, 9 mmol) and the flask was evacuated and back-filled with Ar and sealed. Dioxane (6 mL) was added and the reaction heated at 110 C. overnight. The reaction mixture was cooled to RT and extracted with EtOAc (120 mL). The organic extract was washed sequentially with H2O (10 mL) and brine (10 mL), dried (Na2SO4), filtered and evaporated. The crude product was triturated with Et2O to afford 0.217 g of 45.
 

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