반응 #640616

ord-7446917f366b44adb47d2e8f3352c763

반응 방정식

COc1nc(Br)cnc1N
5-Bromo-3-methoxy-pyrazin-2-ylamine
OB(O)c1ccccc1
phenyl boronic acid
O=C([O-])[O-].[Na+].[Na+]
Na2CO3
COc1nc(-c2ccccc2)cnc1N
product B
수율 82.0%
COc1nc(-c2ccccc2)cnc1N
3-Methoxy-5-phenyl-pyrazin-2-ylamine
수율 82.0%

반응 조건

온도
85°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The reaction mixture was cooled to room temperature
  2. 2
    세척The solution was washed with brine (2×5 mL)
  3. 3
    건조The organic extracts was dried with MgSO4
  4. 4
    기타solvent was removed under vacuum
  5. 5
    기타The residue was purified with flash column

실험 절차

5-Bromo-3-methoxy-pyrazin-2-ylamine (A) (816 mg, 4 mmol) and phenyl boronic acid (732 mg, 6 mmol) in toluene (5 mL), ethanol (5 mL) and Na2CO3 (8 mmol, 1 M aqueous) was purged with nitrogen for 10 minutes, and was added PdCl2(PPh3)2(140 mg, 0.2 mmol). The reaction mixture was stirred at 85° C. for 4 hours. The reaction mixture was cooled to room temperature and diluted with EtOAc (50 mL). The solution was washed with brine (2×5 mL). The organic extracts was dried with MgSO4, then solvent was removed under vacuum. The residue was purified with flash column to give product B (660 mg, 82%) as yellow solid. 1H NMR (400 MHz, CDCl3): δ 8.08 (1H, s), 7.92 (2H, d), 7.46 (3H, m), 4.94 (2H, bs), 4.12 (3H, s); MS: 202 (M+H+).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08048886B2uspto-grants-2011_11