반응 #91314

ord-0d745710e5544d009a976982d437d216

용매

반응 조건

온도
166°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축The solution was concentrated in vacuo
  2. 2
    기타purified by silica gel chromatography (10-20% MeOH/DCM)
  3. 3
    농축The semi-pure fractions were concentrated
  4. 4
    기타to give a pale yellow precipitate, which
  5. 5
    여과was collected by filtration
  6. 6
    기타dried under vacuum

실험 절차

3-Fluoroisonicotinic acid (100 mg, 0.71 mmol), 4-(aminomethyl)-benzonitrile hydrochloride (240 mg, 1.42 mmol), and DIEA (250 μL, 1.42 mmol) were combined in DMA (2 mL) and the reaction mixture was stirred at 166° C. in a microwave for 90 min. The solution was concentrated in vacuo and purified by silica gel chromatography (10-20% MeOH/DCM). The semi-pure fractions were concentrated and then taken up in water to give a pale yellow precipitate, which was collected by filtration and dried under vacuum to give 32 mg (18%) of the title compound. 1H NMR (500 MHz, DMSO-d6): δ 8.10 (br s, 1H), 8.04 (s, 1H), 7.83 (d, 1H, J=5.0 Hz), 7.81 (d, 2H, J=8.0 Hz), 7.58 (d, 1H, J=5.0 Hz), 7.54 (d, 2H, J=8.0 Hz), 4.69 (s, 2H). [M+H] calc'd for C14H11N3O2, 254. found 254.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09447045B2uspto-grants-2016_09