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Phosphorus oxychloride → 6-Bromo-4-chloropyrrolo[1,2-b]pyridazine-3-carbonitrile

HRID 1507901
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HRID 1507901 반응식
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](O)=[C:8]([C:11]#[N:12])[CH:7]=[N:6][N:5]2[CH:13]=1.O=P(Cl)(Cl)[Cl:16]>>[Br:1][C:2]1[CH:3]=[C:4]2[C:9]([Cl:16])=[C:8]([C:11]#[N:12])[CH:7]=[N:6][N:5]2[CH:13]=1
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참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 178510449HCID 178510449, 화합물

생성물 1

HCID 682911366-Bromo-4-chloropyrrolo[1,2-b]pyridazine-3-carbonitrile수율 47.7%

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온도
75 °C

실험 절차

To a 25 mL round bottom flask was added 6-bromo-4-hydroxypyrrolo [1,2-b]pyridazine-3-carbonitrile (16.5 g, 69.47 mmol) and POCl3 (85 mL, 0.88 mol) and the reaction mixture was stirred and heated at 75° C. for 3 hours. The POCl3 was removed under vacuum and the resulting residue was dissolved in CH2Cl2. The solution was cooled to 0° C. and saturated aq. NaHCO3 solution was added and the biphasic mixture was stirred vigorously while allowing to warm to rt. The organic layer was separated and concentrated and the obtained residue was purified by flash silica gel column chromatography to yield 8.5 g (29%) of the title compound as a yellow solid. HPLC (condition P): retention time=16.74 min. 1H NMR (400 MHz, CDCl3) δ ppm: 8.09 (1H, s), 7.94 (1H, d, 2.0 Hz), 7.06 (1H, d, 2.0 Hz).

후처리

  1. customThe POCl3 was removed under vacuum
  2. dissolutionthe resulting residue was dissolved in CH2Cl2
  3. temperatureThe solution was cooled to 0° C.
  4. additionsaturated aq. NaHCO3 solution was added
  5. stirringthe biphasic mixture was stirred vigorously
  6. temperatureto warm to rt
  7. customThe organic layer was separated
  8. concentrationconcentrated
  9. customthe obtained residue was purified by flash silica gel column chromatography

출처 및 근거

ORD 기록
ord-3ac2fc37c1ba48839d9ffc38e9cca150
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09221826B2

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