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Chloroform → HCID 22662826、化合物

HRID 1005733
ノート
印刷プレビュー

反応式

HRID 1005733 の反応式
N[C:2]1[N:7]=[C:6]([C:8]([NH2:10])=[O:9])[C:5]([O:11][CH3:12])=[N:4][CH:3]=1.N([O-])=O.[Na+].C(Cl)(Cl)Cl.[FH:21].N1C=CC=CC=1>>[F:21][C:2]1[N:7]=[C:6]([C:8]([NH2:10])=[O:9])[C:5]([O:11][CH3:12])=[N:4][CH:3]=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

5

反応物 4

HCID 6212ChloroformHCID 64774Pyridine, hydrofluoride (1:1)HCID 226628026-Amino-3-methoxy-2-pyrazinecarboxamideHCID 23668193Sodium Nitrite

生成物 1

HCID 22662826HCID 22662826、化合物

反応条件

温度
10 °C

実験手順

In a nitrogen atmosphere, 1.50 g of 6-amino-3-methoxy-2-pyrazinecarboxamide is dissolved in 12 mL of 70% pyridine hydrofluoride under ice-cooling. Then, 0.71 g of sodium nitrite is added thereto at −50° C., and the resulting solution is stirred at 10° C. for 1 hour. The resulting reaction mixture is stirred at ambient temperature for an additional 1 hour. Thereafter, a mixture of 50 mL of ice water and 100 mL of chloroform is added thereto and the resulting mixture is separated into layers. The organic layer is washed with saturated aqueous solution of sodium chloride and saturated aqueous solution of sodium hydrogen carbonate, and dried over anhydrous magnesium sulfate. Then, the solvent is distilled off under reduced pressure to obtain 1.29 g of 6-fluoro-3-methoxy-2-pyrazinecarboxamide.

後処理

  1. temperaturecooling
  2. customThe resulting reaction mixture
  3. stirringis stirred at ambient temperature for an additional 1 hour
  4. additionis added
  5. customthe resulting mixture is separated into layers
  6. washThe organic layer is washed with saturated aqueous solution of sodium chloride and saturated aqueous solution of sodium hydrogen carbonate
  7. dry with materialdried over anhydrous magnesium sulfate
  8. distillationThen, the solvent is distilled off under reduced pressure

出典と根拠

ORDレコード
ord-eb4b04853cd140cab253dec460e39aa9
出典データセット
uspto-grants-2004_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06787544B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート