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

HRID 1507901
ノート
印刷プレビュー

反応式

HRID 1507901 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 24813Phosphorus oxychlorideHCID 178510449HCID 178510449、化合物

生成物 1

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

反応条件

温度
75 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-3ac2fc37c1ba48839d9ffc38e9cca150
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09221826B2

反応ノート

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