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Chemical Structure| 1262015-14-4 Chemical Structure| 1262015-14-4

Structure of 1262015-14-4

Chemical Structure| 1262015-14-4

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Product Details of [ 1262015-14-4 ]

CAS No. :1262015-14-4
Formula : C17H21BN2O4
M.W : 328.17
SMILES Code : O=C(N1C=CN=C1)OCC2=CC=C(B3OC(C)(C)C(C)(C)O3)C=C2

Safety of [ 1262015-14-4 ]

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 [ 1262015-14-4 ]

* 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 [ 1262015-14-4 ]

[ 1262015-14-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 530-62-1 ]
  • [ 302348-51-2 ]
  • [ 1262015-14-4 ]
YieldReaction ConditionsOperation in experiment
85% In dichloromethane; at 20℃;Inert atmosphere; Compound 2 (660 mg, 2.82 mmol) was dissolved in 10 mL of dry CH2Cl2.Then, N,N'-carbonyldiimidazole (915 mg, 5.64 mmol) was added, and the mixture was stirred at room temperature for 1-2 h under N2. After the reaction was completed, 40 ml of CH 2 Cl 2 was added, and the mixture was washed three times with an equal amount of 1 M HCl solution, and the organic phase was dried over anhydrous sodium sulfate.Concentrated under reduced pressure to give a white solid 787mg, yield 85%.
In dichloromethane; at 20℃; for 2h; 2.07 g of 1,1'-carbonyldiimidazole and 2.07 g of 4- (hydroxymethyl) phenylboronic pinicole ester(4- (hydroxymethyl) phenylboronic acid pinacol ester) was dissolved in 20 mL of dichloromethane (DCM)And allowed to react at room temperature for 2 hours. The product was named 1 and 1 was obtained by silica gel chromatography using an eluent of 1: 1 mixture of ethyl acetate and hexane.
  • 2
  • [ 288-32-4 ]
  • [ 32315-10-9 ]
  • [ 302348-51-2 ]
  • [ 1262015-14-4 ]
  • 3
  • [ 302348-51-2 ]
  • [ 1262015-14-4 ]
 

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