تفاعل #1897

ord-b73af90813ea458ca97a1404afcbed16

معادلة التفاعل

Nc1ccc(Br)cc1-c1cccnc1C(=O)c1ncccc1-c1cc(Br)ccc1N
2-amino-5-bromophenyl-2-pyridylketone
CO
methanol
[BH4-].[Na+]
sodium borohydride
Nc1ccc(Br)cc1C(O)c1ccccn1
2-amino-5-bromo-α-(2-pyridyl)benzyl alcohol

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe solvent methanol was evaporated off under reduced pressure
  2. 2
    workup.ADDITIONThe residue was treated with an aqueous solution of hydrochloric acid
  3. 3
    استخلاصextracted with ethyl acetate
  4. 4
    غسيلThe ethyl acetate layer was washed with water
  5. 5
    تجفيفdried over anhydrous magnesium sulfate
  6. 6
    تركيزconcentrated under reduced pressure
  7. 7
    أخرىThe residue was purified by silica gel column chromatography (eluent, hexane:ethyl acetate=2:1)

الإجراء التجريبي

In 100 ml of methanol was dissolved 10 g of 2-amino-5-bromophenyl-2-pyridylketone. To the solution was added 1.7 g of sodium borohydride and stirred for 30 minutes. The solvent methanol was evaporated off under reduced pressure. The residue was treated with an aqueous solution of hydrochloric acid. The decomposed residue was then neutralized with 200 ml of a sodium bicarbonate aqueous solution, and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent, hexane:ethyl acetate=2:1) to give 2-amino-5-bromo-α-(2-pyridyl)benzyl alcohol (9.0 g) as prisms, m.p. 104°-105° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05726306uspto-grants-1998_03