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Chemical Structure| 945865-21-4 Chemical Structure| 945865-21-4

Structure of 945865-21-4

Chemical Structure| 945865-21-4

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Product Details of [ 945865-21-4 ]

CAS No. :945865-21-4
Formula : C16H21BN2O4
M.W : 316.16
SMILES Code : O=C(C1=CC2=C(B3OC(C)(C)C(C)(C)O3)C=CN=C2N1)OCC
MDL No. :MFCD11617868

Safety of [ 945865-21-4 ]

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 [ 945865-21-4 ]

* 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 [ 945865-21-4 ]

[ 945865-21-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 942920-55-0 ]
  • [ 73183-34-3 ]
  • [ 945865-21-4 ]
YieldReaction ConditionsOperation in experiment
68% With potassium acetate;(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In N,N-dimethyl-formamide; at 90℃; for 48h; A mixture of <strong>[942920-55-0]ethyl 4-bromo-1H-pyrrolo[2,3-b]pyridine-2-carboxylate</strong> (1.0 g, 3.9 mmol), 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi-1,3,2-dioxaborolane (2.1 g, 7.8 mmol), KOAc (1.2 g, 11.7 mmol) and Pd(dppf)Cl2 (0.3 g, 0.4 mmol) in DMF (20 mL) was heated at 90 C. for 48 h under inert atmosphere. After cooling to rt, the reaction was quenched by aqueous NH4Cl. The resulting mixture was extracted with AcOEt. The organic layer was washed with brine, water, and dried over sodium sulfate. Concentration in vacuo gave the residue, which was purified by YAMAZEN Fast Flow Liquid Chromatography (silica gel, EtOAc:hexane=1:1) to give the desired product as a white solid (0.8 g, 68%). 1H NMR (400 MHz, DMSO-d6) ppm 1.33-1.37 (m, 15H), 4.37 (q, 2H, J=7.1 Hz), 7.29 (d, 1H, J=2.0 Hz), 7.40 (d, 1H, J=4.5 Hz), 8.44 (d, 1H, J=4.3 Hz), 12.55 (brs, 1H). MS (ESI): m/z 315 (M-1)-, 317 (M+1)+
68% With potassium acetate;dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; In N,N-dimethyl-formamide; at 90℃; for 48h; Ethyl 4-bromo-1 H-pyrrolo[2,3-6]pyridine-2-carboxylate (1.0 g, 3.9 mmol), 4l4,4',4',5,5,5',5'-octamethyl-2,2'-bi-1,3,2-dioxaborolane (2.1 g, 7.8 mmol), KOAc (1.2 g, 11.7 mmol) and Pd(dppf)CI2 (0.3 g, 0.4 mmol) in DMF (20 ml_) was heated at 90 0C for 48 h under inert atmosphere. After cooling to rt, the reaction was quenched with aqueous NH4CI. The resulting mixture was extracted with AcOEt. The organic layer was washed by water, brine, and dried over sodium sulfate. Concentration in vacuo gave the residue, which was purified by YAMAZEN Fast Flow Liquid Chromatography (silica gel, EtOAc.hexane , 1:1) to give the desired product as a white solid (0.8 g, 68 %). 1H NMR (400MHz, DMSO-d6) ppm 1.33- <n="98"/>1.37 (m, 15H), 4.37 (q, 2H, J = 7.1 Hz), 7.29 (d, 1 H1 J = 2.0 Hz), 7.40 (d, 1 H1 J = 4.5 Hz), 8.44 (d, 1 H, J = 4.3 Hz), 12.55 (brs, 1 H). LC/MS: m/z 315 (M-1 )-, 317 (M+1)+.
 

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