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Acetic Acid Mixture with Hydrobromic Acid → HCID 178515741、化合物

HRID 1799578
ノート
印刷プレビュー

反応式

HRID 1799578 の反応式
[NH2:1][C:2]1[C:3](/[CH:9]=[CH:10]/[C:11]([O:13]CC)=O)=[N:4][C:5](I)=[N:6][CH:7]=1.[BrH:16].C(O)(=O)C>>[Br:16][C:5]1[N:6]=[CH:7][C:2]2[N:1]=[C:11]([OH:13])[CH:10]=[CH:9][C:3]=2[N:4]=1
参加物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 21893785Acetic Acid Mixture with Hydrobromic AcidHCID 58216629(E)-Ethyl 3-(5-amino-2-iodopyrimidin-4-yl)acrylate

生成物 1

HCID 178515741HCID 178515741、化合物

実験手順

A 3-necked roundbottom flask, was charged with (E)-ethyl 3-(5-amino-2-iodopyrimidin-4-yl)acrylate (120 g, 388 mmol) followed by hydrogen bromide/acetic acid (1500 ml). The resulting solution was allowed to react, with stirring, for 1.5 hours while the temperature was maintained at 40˜50° C. Upon completion, the mixture was concentrated under reduced pressure. The resulting residue was dissolved in 500 ml of methanol and the pH was adjusted to 7 by the addition of sodium bicarbonate. The resulting mixture was washed once with a solution of 46 g of NaHSO3 in 200 mL of water. The organic layer was concentrated under reduced pressure. The resulting slurry was filtered and the solids collected to afford the title compound.

後処理

  1. customto react
  2. temperature
was maintained at 40˜50° C
  • concentrationUpon completion, the mixture was concentrated under reduced pressure
  • dissolutionThe resulting residue was dissolved in 500 ml of methanol
  • additionthe pH was adjusted to 7 by the addition of sodium bicarbonate
  • washThe resulting mixture was washed once with a solution of 46 g of NaHSO3 in 200 mL of water
  • concentrationThe organic layer was concentrated under reduced pressure
  • filtrationThe resulting slurry was filtered
  • customthe solids collected
  • 出典と根拠

    ORDレコード
    ord-0929379065494829aa1ea04b07d38cc3
    出典データセット
    uspto-grants-2013_01
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US08344144B2

    反応ノート

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