تفاعل #490290

ord-411ea62c61174dc49dd3ea8cb1003752

معادلة التفاعل

COc1ccccc1CCl
2-methoxybenzyl chloride
NCc1ccccn1
2-(Aminomethyl)pyridine
O=C([O-])[O-].[K+].[K+]
potassium carbonate
COc1ccccc1CNCc1ccccn1
N-(2-methoxybenzyl)-1-(pyridin-2-yl)methanamine

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe solvent was evaporated
  2. 2
    workup.DISSOLUTIONthe residual oil was dissolved in CH2Cl2 (75 mL)
  3. 3
    استخلاصextracted with water (75 mL×3)
  4. 4
    أخرىthe resulting yellow-orange oil was purified by silica gel chromatography
  5. 5
    غسيلeluting with CH2Cl2

الإجراء التجريبي

2-methoxybenzyl chloride (1.50 g, 9.5 mmol) and 2-(Aminomethyl)pyridine (5.18 g, 47 mmol) were dissolved in 800 mL CH3CN. To this solution was added potassium carbonate (1.324 g, 9.5 mmol) and the mixture was stirred at room temperature for three days. The solvent was evaporated, and the residual oil was dissolved in CH2Cl2 (75 mL) and extracted with water (75 mL×3). The combined CH2Cl2 layers were reduced in volume, and the resulting yellow-orange oil was purified by silica gel chromatography eluting with CH2Cl2, followed by a 3% (NH3)MeOH/97% CH2Cl2 solution (62%). 1H NMR (CDCl3) δ 8.520 (dd, 1H, Ar), 7.600 (m, 1H, Ar), 7.335 (d, 1H, Ar), 7.27 (d, 1H, Ar), 7.211 (t, 1H, Ar), 7.113 (m, 1H, Ar), 6.895 (t, 1H, Ar), 6.832 (d, 1H, Ar), 3.921 (s, 2H, —CH2—), 3.864 (s, 2H, —CH2—), 3.800 (s, 3H, —OCH3), 3.043 (s(br), 1H, —CH—). Mass Spec.=229.13 (M+H)+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08747810B2uspto-grants-2014_06