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Phosphorus oxychloride → 2-Chloro-6-fluoroimidazo[1,2-A]pyridine

HRID 705068
ノート
印刷プレビュー

反応式

HRID 705068 の反応式
Br.[NH:2]=[C:3]1[CH:8]=[CH:7][C:6]([F:9])=[CH:5][N:4]1[CH2:10][C:11](OCC)=O.P(Cl)(Cl)([Cl:18])=O>>[Cl:18][C:11]1[N:2]=[C:3]2[CH:8]=[CH:7][C:6]([F:9])=[CH:5][N:4]2[CH:10]=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 70497293Ethyl 2-(5-fluoro-2-iminopyridin-1(2H)-yl)acetate hydrobromide

生成物 1

HCID 552678642-Chloro-6-fluoroimidazo[1,2-A]pyridine

反応条件

温度
105 °C

実験手順

A mixture of ethyl 2-imino-5-fluoro-1,2-dihydropyridine-1-yl-acetate hydrobromide (4.12 g, 14.76 mmol) in phosphorus oxychloride (68.8 mL, 738 mmol) was heated at 105° C. for 2 hours. The mixture was then cooled to room temperature and concentrated under reduced pressure. To the resulting residue were added ice water and ammonium hydroxide until the pH of the solution was 8. The solution was then extracted with dichloromethane. The organic extracts were combined, dried over MgSO4, filtered and concentrated under reduced pressure. Purification by flash chromatography on silica gel (30% ethyl acetate in hexanes) provided the title compound: LCMS m/z 170.96 [M+H]+, 172.79 [M+2+H]+; 1H NMR (500 MHz, CDCl3) δ 8.00 (s, 1H), 7.53-7.50 (m, 2H), 7.18-7.13 (m, 1H).

後処理

  1. temperatureThe mixture was then cooled to room temperature
  2. concentrationconcentrated under reduced pressure
  3. additionTo the resulting residue were added ice water and ammonium hydroxide until the pH of the solution
  4. extractionThe solution was then extracted with dichloromethane
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customPurification by flash chromatography on silica gel (30% ethyl acetate in hexanes)

出典と根拠

ORDレコード
ord-d28c65fd66664dee80a943d003b1a6e9
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09173873B2

反応ノート

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