5-(4-[1,3]Dioxolan-2-yl-2-fluorophenoxy)pyrazine-2-carboxamide → 5-(2-Fluoro-4-formylphenoxy)pyrazine-2-carboxamide

HRID 228438ノート

反応式

HRID 228438 の反応式
[O:1]1CCO[CH:2]1[C:6]1[CH:21]=[CH:20][C:9]([O:10][C:11]2[N:12]=[CH:13][C:14]([C:17]([NH2:19])=[O:18])=[N:15][CH:16]=2)=[C:8]([F:22])[CH:7]=1>C(O)=O>[F:22][C:8]1[CH:7]=[C:6]([CH:2]=[O:1])[CH:21]=[CH:20][C:9]=1[O:10][C:11]1[N:12]=[CH:13][C:14]([C:17]([NH2:19])=[O:18])=[N:15][CH:16]=1

参加物

3

反応物 1

HCID 597302115-(4-[1,3]Dioxolan-2-yl-2-fluorophenoxy)pyrazine-2-carboxamide

生成物 1

HCID 597300135-(2-Fluoro-4-formylphenoxy)pyrazine-2-carboxamide収率 75.7%

試薬・触媒・溶媒 1

HCID 284Formic Acid溶媒

実験手順

Combine formic acid (90%, 453 mL) and crude 5-(4-[1,3]dioxolan-2-yl-2-fluorophenoxy)pyrazine-2-carboxamide (Example 737, Part D) (32.81 g, approximately 0.09 mole) and stir initially a clear yellow solution, which becomes a thick slurry in an hour at room temperature. Stir overnight at room temperature till the reaction complete by HPLC. Quench the reaction with deionized water (1 L) and extract with dichloromethane (4×4 L). Combine the extracts and mix with aqueous sodium bicarbonate solution. Concentrate on a rotary evaporator to give a slurry of a solid in water (when the separation of layers not possible). Extract the mixture with ethyl acetate (4×1 L) and concentrate the combined extracts to a yellow solid (29.65 g). Form slurries successively four times with boiling methanol (1 L) and filter while hot. Combine the filter cakes and dissolve in enough boiling methanol to give a clear solution. Concentrate the solution to approximately 1 liter and allow to crystallize at 0° C. Filter the resulting slurry at 0° C. and dry the filter cake under vacuum at room temperature to give the title compound (17.79 g, 75.7%). 1H NMR (DMSO-d6) δ 7.70 (t, 1H, ArH), 7.78 (s, 1H. HetH), 7.86-7.93 (m, 2H, ArH), 8.14 (s, 1H, HetH), 8.73 (d, 2H, amide), 10.0 S, 1H, CHO); 13C NMR (DMSO-d6) δ 116.884, 124.606, 126.980, 133.186, 134.967, 140.765, 144.016, 152.493, 154.974, 159.276, 164.057, 190.777; MS (ES+) m/z 262.3 (M+H).

後処理

  1. customin an hour
  2. customat room temperature
  3. customQuench
  4. customthe reaction with deionized water (1 L)
  5. extractionextract with dichloromethane (4×4 L)
  6. additionCombine the extracts and mix with aqueous sodium bicarbonate solution
  7. concentrationConcentrate on a rotary evaporator
  8. customto give a slurry of a solid in water (when
  9. customthe separation of layers not possible)
  10. extractionExtract the mixture with ethyl acetate (4×1 L)
  11. concentrationconcentrate the combined extracts to a yellow solid (29.65 g)
  12. filtrationForm slurries successively four times with boiling methanol (1 L) and filter while hot
  13. dissolutionCombine the filter cakes and dissolve
  14. customto give a clear solution
  15. concentrationConcentrate the solution to approximately 1 liter
  16. customto crystallize at 0° C
  17. filtrationFilter the resulting slurry at 0° C.
  18. customdry the filter cake under vacuum at room temperature

出典と根拠

ORDレコード
ord-570cc4f90c28438c9a052b23c667885a
出典データセット
uspto-grants-2009_07
特許番号
US07560463B2

反応ノート

読み込み中…