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Chemical Structure| 51239-46-4 Chemical Structure| 51239-46-4

Structure of 51239-46-4

Chemical Structure| 51239-46-4

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Product Details of [ 51239-46-4 ]

CAS No. :51239-46-4
Formula : C7H10BNO2
M.W : 150.97
SMILES Code : NCC1=CC=C(B(O)O)C=C1
MDL No. :MFCD06213214

Safety of [ 51239-46-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P280-P305+P351+P338-P310

Application In Synthesis of [ 51239-46-4 ]

* 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 [ 51239-46-4 ]

[ 51239-46-4 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 51239-46-4 ]
  • [ 489446-42-6 ]
YieldReaction ConditionsOperation in experiment
For compounds (2-6) the commercially available 4-aminomethylphenylboronic acid and 3-aminomethylphenylboronic acid were BOC protected under standard conditions (Wei et al., 2000) and the appropriate boronic acid was used at the Suzuki coupling stage in the synthesis of compounds (2-6). The BOC group was removed with 4 M HCl in dioxane at RT after hydrazone coupling;
  • 2
  • [ 24424-99-5 ]
  • [ 51239-46-4 ]
  • [ 489446-42-6 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In tetrahydrofuran; for 1h;Heating / reflux; 3,5-Dimethyl-isoxazole-4-sulfonic acid 4-(5-fluoro-2-methoxy-pyridin-3-yl) benzylamide Di-tert-butyl dicarbonate (3.5 g, 16 mmol) and triethylamine (13 ml, 9.4 mmol) were added to a stirred solution of 4-aminomethylphenylboronic acid (3 g, 16 mmol) in tetrahydrofuran (100 ml). The reaction was stirred under reflux for 1 hour, then the solvent evaporated and the residue partitioned between water and ethyl acetate. The organic phase was concentrated under reduced pressure to give tert-butoxycarbonylaminomethyl-4-phenyl-boronic acid (2.67 g, 10.6 mmol) as a white solid. Toluene (16 ml), ethanol (4 ml), 2M sodium carbonate solution and tetrakis(triphenylphosphine) palladium (0) were added to tert-butoxycarbonylaminomethyl-4-phenyl-boronic acid (1.349 g, 5.4 mmol) and 3-bromo-5-fluoro-2-methoxy-pyridine (0.505 g, 2.45 mmol) and the mixture stirred under reflux for 24 h. Water was added and the mixture extracted with ethyl acetate. The organic phase was separated and the solvent evaporated. The residue was purified on silica gel eluting with 3:1 heptane/ethyl acetate to give [4-(5-fluoro-2-methoxy-pyridin-3-yl-benzyl]-carbamic acid-tert-butyl ester as a yellow oil. Trifluoroacetic acid (2 ml, 0.026 mmol) was added to a solution of [4-(5-fluoro-2-methoxy-pyridin-3-yl-benzyl]-carbamic acid-tert-butyl ester (0.8 g, 2.41 mmol) in dichloromethane (4 ml) and the reaction mixture stirred for 2 h. The solvent was evaporated and the residue partitioned between water and ethyl acetate. The organic phase was separated and the solvent evaporated to give 4-(5-fluoro-2-methoxy-pyridin-3-yl)-benzylamine. The title compound was prepared in a similar manner to N-[1-(2-allyl-5'-fluoro-2'-methoxy-biphenyl-4-yl)-ethyl]-3,4-difluoro-benzenesulfonamide (Example 34) using 4-(5-fluoro-2-methoxy-pyridin-3-yl)-benzylamine and 3,5-dimethyl-isoxazole-4-sulfonyl chloride. MS (ESI) m/z: 392 [M+H]+.
With triethylamine; In tetrahydrofuran; at 20℃; for 1h; To a solution of 4-aminomethylphenylboronic acid (2.65 mmol) in THF (10 mL) were added di-tert-butyl dicarbonate (3.97 mmol) and triethylamine (1 mL). The mixture was stirred at room temperature for 1 h. After completion of the reaction, excess solvent was evaporated to dryness under reduced pressure. The residue was diluted with water (30 mL) and ethyl acetate (15 mL). The organic phase was separated, dried over MgSO4, filtered, and concentrated under reduced pressure. The NHBoc-protected boronic acid was then used for Suzuki coupling as described in compound 6 to afford compound 9.
  • 3
  • [ 5467-57-2 ]
  • [ 51239-46-4 ]
  • [ 1312812-93-3 ]
YieldReaction ConditionsOperation in experiment
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In 1,4-dioxane; water; at 140℃; for 0.25h;Inert atmosphere; Microwave irradiation; General procedure: 2-Chloroquinoline-4-carboxylic acid (0.15 g, 0.72 mmol), 3,5-dimethylisoxazole-4-boronic acid (0.12 g, 0.87 mmol) and Pd(PPh3)4 (42 mg, 0.04 mmol) were added to a mixture of dioxane (2 mL) and a 1 M aq solution of K2CO3 (2 mL). The reaction mixture was degassed, sealed, and heated in a microwave reactor at 140 °C for 15 min. The reaction mixture was concentrated in vacuo to leave a residue which was purified by HPLC using a gradient of 30-100percent mobile phase A (100percent CH3CN) over 30 min (mobile phase B = 5percent CH3CN + 95percent 0.1 M NH4OAc) to give the intermediate carboxylic acid (148 mg, 75percent).
  • 4
  • [ 489446-42-6 ]
  • [ 51239-46-4 ]
 

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