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Acetic Anhydride → 6-Bromo-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile

HRID 1253459
ノート
印刷プレビュー

反応式

HRID 1253459 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([O:14][CH3:15])[C:5]2[N:6]([N:8]=[CH:9][C:10]=2[CH:11]=[N:12]O)[CH:7]=1.C(OC(=O)C)(=O)C>>[Br:1][C:2]1[CH:3]=[C:4]([O:14][CH3:15])[C:5]2[N:6]([N:8]=[CH:9][C:10]=2[C:11]#[N:12])[CH:7]=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 7918Acetic AnhydrideHCID 866570506-Bromo-4-methoxypyrazolo[1,5-a]pyridine-3-carbaldehyde oxime

生成物 1

HCID 584048986-Bromo-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile

反応条件

温度
50 °C

実験手順

The oxime isomer mixture of 6-bromo-4-methoxypyrazolo[1,5-a]pyridine-3-carbaldehyde oxime (85.0 mg, 0.315 mmol) was suspended in acetic anhydride (3.0 ml, 31.8 mmol) and heated to 50° C. for 3 h to give a pale blue solution. The solution was then heated to 75° C. for 2 h to give a dark blue solution. The solution was then heated to 100° C. overnight to give a dark purple mixture. The reaction mixture was concentrated and the residue was diluted in ethyl acetate, washed with saturated aqueous sodium hydrogen carbonate and brine then dried over sodium sulfate, filtered and concentrated. The residue was purified by column chromatography on silica gel (ethyl acetate/isohexane gradient) to give 6-bromo-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile.

後処理

  1. customto give a pale blue solution
  2. temperatureThe solution was then heated to 75° C. for 2 h
  3. customto give a dark blue solution
  4. temperatureThe solution was then heated to 100° C. overnight
  5. customto give a dark purple mixture
  6. concentrationThe reaction mixture was concentrated
  7. additionthe residue was diluted in ethyl acetate
  8. washwashed with saturated aqueous sodium hydrogen carbonate and brine
  9. dry with materialthen dried over sodium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated
  12. customThe residue was purified by column chromatography on silica gel (ethyl acetate/isohexane gradient)

出典と根拠

ORDレコード
ord-76fa1095a8af4e38904b1c110ac573ee
出典データセット
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08455477B2

反応ノート

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