반응 #57784

ord-7505e72185284a5d9da00d99b64cd23e

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas added in one portion to the solution
  2. 2
    기타prepared
  3. 3
    workup.STIRRINGThe reaction mixture was stirred for 2 hrs at 0° C.
  4. 4
    workup.STIRRINGwith stirring
  5. 5
    기타The resulting two-phase system was separated
  6. 6
    추출extracted with ethyl acetate (2×150 ml)
  7. 7
    추출The combined organic extractions
  8. 8
    건조were dried over Na2SO4
  9. 9
    기타After removal of solvent
  10. 10
    기타the residue was purified by the flash chromatography
  11. 11
    기타Crystallization of the product from Et2O/hexane mixture

실험 절차

To a solution of 2-bromopyridine (5 ml, 52 mmol) in Et2O (60 ml) was added 40 ml of a n-butyllithium (1.6M in hexane, 64 mmol) drop wise at −40° C. over 30 min under a nitrogen atmosphere. The resulting yellow solution was stirred for a further 1 hr at −50° C. to −30° C. In a separate flask, a solution of 2-amino-5-chlorobenzoic acid (2.05 g, 12 mmol) in dry THF (90 ml), under nitrogen atmosphere and with ice-cooling, was added in one portion to the solution prepared as described above. The reaction mixture was stirred for 2 hrs at 0° C. and then chlorotrimethylsilane (30 ml) was added at 0° C. with stirring. The reaction mixture was allowed to warm to room temperature and 1 N HCl aq (100 ml) was added. The resulting two-phase system was separated. The aqueous phase was adjusted to pH12 with 6N NaOH solution and extracted with ethyl acetate (2×150 ml). The combined organic extractions were dried over Na2SO4. After removal of solvent, the residue was purified by the flash chromatography using ethyl acetate/hexane (1:4) as eluent. Crystallization of the product from Et2O/hexane mixture gave 1.26 g (45%) of desired product as yellow solid. 1H-NMR (DMSO-d6, 500 MHz): δ 6.90 (1H, d, J=9 Hz), 7.31 (1H, dd, J=9 and 2.5 Hz), 7.40 (2H, br), 7.53 (1H, d, J=2.5 Hz), 7.61 (1H, m), 7.79 (1H, d, J=8 Hz), 8.03 (1H, m), 8.69 (1H, m). MS: (ESI+): 233.2 (M+1).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07420055B2uspto-grants-2008_09