تفاعل #68414

ord-47dd9896f15c4e0d94e5438076d71229

معادلة التفاعل

N.O
NH3.H2O
NCc1cc(F)c(Cl)nc1Cl
(2,6-dichloro-5-fluoropyridin-3-yl)methanamine
NCc1cc(F)c(Cl)nc1Cl
Compound 144
NCc1cc(F)c(Cl)nc1Cl
(2,6-dichloro-5-fluoropyridin-3-yl)methanamine
NCc1cncc(F)c1
title compound
NCc1cncc(F)c1
(5-Fluoropyridin-3-yl)methanamine

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىTo a Parr reaction bottle
  2. 2
    ترشيحfiltered
  3. 3
    تركيزconcentrated
  4. 4
    استخلاصextracted with EtOAc (×3)
  5. 5
    غسيلThe combined organic layer was washed with brine
  6. 6
    تجفيفdried over Na2SO4
  7. 7
    تركيزconcentrated in vacuo
  8. 8
    workup.DISTILLATIONThe crude product was purified by distillation under vacuum

الإجراء التجريبي

To a Parr reaction bottle was added Pd—C (10%, 560 mg, 0.52 mmol), followed by 28% NH3.H2O (50 ml) and a solution of (2,6-dichloro-5-fluoropyridin-3-yl)methanamine (Compound 144, 10.1 g, 52 mmol) in MeOH (100 ml). The mixture was placed under 51 psi H2 on a shaker type Parr apparatus for 16 h, filtered and concentrated. The resulting aqueous solution was basified with NaOH, extracted with EtOAc (×3). The combined organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The crude product was purified by distillation under vacuum to yield the title compound as colorless oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08524917B2uspto-grants-2013_09