Tetrafluoroboric acid → 5-Bromo-8-fluoroisoquinoline

HRID 2098086노트

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HRID 2098086 반응식
N[C:2]1[CH:3]=[CH:4][C:5]([Br:12])=[C:6]2[C:11]=1[CH:10]=[N:9][CH:8]=[CH:7]2.N([O-])=O.[Na+].[H+].[B-](F)(F)(F)[F:19]>>[Br:12][C:5]1[CH:4]=[CH:3][C:2]([F:19])=[C:11]2[C:6]=1[CH:7]=[CH:8][N:9]=[CH:10]2

참가 물질

4

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온도
0 °C

실험 절차

To a solution of 8-amino-5-bromoisoquinoline in 48% HBF4 (30 mL) at 0° C. was slowly added an aqueous (10 mL) solution of NaNO2 (172 mg, 2.5 mmol). The reaction mixture was stirred at 0° C. for 1 h and was then concentrated under reduced pressure to give a dark residue. The dark residue was heated to 150° C. for 16 h. The resulting dark oil was cooled to 23° C., quenched with ammonium hydroxide and extracted with DCM. The organic solution was concentrated and the resulting dark solid was recrystallized from EtOAc/Hexanes. The desired product (100 mg) was in the mother liquor while the by-product was filtered away as a solid. LCMS showed an m/z of 228.0/226.0 with a retention time of 1.318 min, method [1].

후처리

  1. concentrationwas then concentrated under reduced pressure
  2. customto give a dark residue
  3. temperatureThe dark residue was heated to 150° C. for 16 h
  4. temperatureThe resulting dark oil was cooled to 23° C.
  5. customquenched with ammonium hydroxide
  6. extractionextracted with DCM
  7. concentrationThe organic solution was concentrated
  8. customthe resulting dark solid was recrystallized from EtOAc/Hexanes
  9. filtrationwas filtered away as a solid

출처 및 근거

ORD 기록
ord-1d5c8005f2384d548fdce427af38c67b
출처 데이터셋
uspto-grants-2013_05
특허 번호
US08450363B2

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