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Chemical Structure| 144650-00-0

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Product Details of [ 144650-00-0 ]

CAS No. :144650-00-0
Formula : C8H9BrN2O
M.W : 229.07
SMILES Code : N=C(N)C1=CC(Br)=CC=C1OC

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Application In Synthesis of [ 144650-00-0 ]

* 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 [ 144650-00-0 ]

[ 144650-00-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 144649-99-0 ]
  • [ 144650-00-0 ]
YieldReaction ConditionsOperation in experiment
43% A 1 M solution of lithium bis-hexamethylsilazide (220 mmol, 220 mL) in tetrahydrofuran was transferred into a 3 neck round bottom flask. The solution was cooled to 0° C. and treated dropwise with <strong>[144649-99-0]5-bromo-2-methoxy-benzonitrile</strong> (100 mmol 21.21 g) in tetrahydrofuran over 20 minutes. The reaction mixture was allowed to stir at 0° C. for 30 minutes, then allowed to stir at room temperature for 4 hours. The reaction mixture was cooled to 0° C. and treated with 2 M hydrochloric acid (350 mL) dropwise. The reaction mixture was allowed to stir for 15 hours at room temperature and poured into a separating funnel. The layers were separated and the organics were washed with 2 M hydrochloric acid (100 mL). The aqueous layer was treated with 2 M NaOH solution (400 mL). The aqueous layer was extracted with 3.x.200 mL of chloroform. The organics were dried with MgSO4, filtered, and evaporated to give a dark yellow solid. This was triturated with diethyl ether to provide the title compound as a yellow solid. Yield 9.8 g, 43percent. Analytical LCMS method 2, retention time 0.40 min, M+H=229. 1H NMR: (CDCl3) delta: 7.71 (d, 1H), 7.46 (dd, 1H), 6.83 (d, 1H), 5.48 (br, s, 3H), 3.86 (s, 3H).
silica gel; In methanol; dichloromethane; EXAMPLE II A mixture of 4.0 g <strong>[144649-99-0]5-bromo-2-methoxybenzonitrile</strong>, 5 g 3A molecular sieves and 60 mL of anhydrous methanol was saturated with HCl gas at 0° C. and allowed to stand at 0° C. for 24 h. The solvent was removed in vacuo and the residue taken up in 75 mL of anhydrous methanol and saturated with ammonia gas at room temperature. The reaction mixture was then heated at 80° C. for 4 h in a sealed tube. The sovent was removed in vacuo, the reaction mixture was diluted with 3N HCl and washed with ethyl acetate to remove unreacted nitrile. The aqueous layer was made basic with 50percent NaOH and the product was extracted three times with 10percent methanol in methylene chloride. The combined organic extracts were dried over potassium carbonate and the solvents removed in vacuo to afford 5-bromo-2-methoxybenzamidine as a glassy solid.
silica gel; In methanol; dichloromethane; EXAMPLE II STR32 A mixture of <strong>[144649-99-0]5-Bromo-2-methoxy-benzonitrile</strong> (4.0 g), 3A molecular sieves (5 g) and anhydrous methanol (60 mL) was saturated with HCl gas at room temperature and allowed to stand at room temperature for 24 h. The solvent was removed in, vacuo and the residue taken up in 75 mL of anhydrous methanol and saturated with ammonia gas at room temperature. The reaction mixture was then heated at 80° C. for 4 h in a sealed tube. The solvent was removed in vacuo, the reaction mixture was diluted with 3N HCl and washed with ethyl acetate to remove unreacted nitrile. The aqueous layer was made basic with 50percent NaOH and the product was extracted three times with 10percent methanol in methylene chloride. The combined organic extracts were dried over magnesium sulfate and the sovents removed in vacuo to afford 5-Bromo-2-methoxy-benzamidine as a glassy solid.
In methanol; dichloromethane; EXAMPLE II STR35 A mixture of <strong>[144649-99-0]5-Bromo-2-methoxy-benzonitrile</strong> (4.0 g), 3A molecular selves (5 g) and anhydrous methanol (60 mL) was saturated with HCl gas at room temperature and allowed to stand at room temperature for 24 h. The solvent was removed in vacuo and the residue taken up in 75 mL of anhydrous methanol and saturated with ammonia gas at room temperature. The reaction mixture was then heated at 80° C. for 4 h in a sealed tube. The sovent was removed in vacuo, the reaction mixture was diluted with 3N HCl and washed with ethyl acetate to remove unreacted nitrile. The aqueous layer was made basic with 50percent NaOH and the product was extracted three times with 10percent methanol in methylene chloride. The combined organic extracts were dried over magnesium sulfate and the sovents removed in vacuo to afford 5-Bromo-2-methoxy-benzamidine as a glassy solid. STR36
silica gel; In methanol; dichloromethane; EXAMPLE II STR22 A mixture of <strong>[144649-99-0]5-Bromo-2-methoxy-benzonitrile</strong> (4.0 g), 3A molecular sieves (5 g) and anhydrous methanol (60 mL) was saturated with HCl gas at room temperature and allowed to stand at room temperature for 24 h. The solvent was removed in vacuo and the residue taken up in 75 mL of anhydrous methanol and saturated with ammonia gas at room temperature. The reaction mixture was then heated at 80° C. for 4 h in a sealed tube. The solvent was removed in vacuo, the reaction mixture was diluted with 3N HCl and washed with ethyl acetate to remove unreacted nitrile. The aqueous layer was made basic with 50percent NaOH and the product was extracted three times with 10percent methanol in methylene chloride. The combined organic extracts were dried over magnesium sulfate and the solvents removed in vacuo to afford 5-Bromo-2-methoxy-benzamidine as a glassy solid.

 

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