Trifluoroacetic anhydride → 4-Chloro-6-methoxy-quinoline-3-carbonitrile

HRID 638970ノート

反応式

HRID 638970 の反応式
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([O:12][CH3:13])[CH:10]=2)[N:5]=[CH:4][C:3]=1[C:14]([NH2:16])=O.C(OC(C(F)(F)F)=O)(C(F)(F)F)=O>C(Cl)Cl.CCN(CC)CC>[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([O:12][CH3:13])[CH:10]=2)[N:5]=[CH:4][C:3]=1[C:14]#[N:16]

参加物

5

実験手順

To a suspension of 4-chloro-6-(methyloxy)-3-quinolinecarboxamide (0.92 g, 3.9 mmol) in CH2Cl2 (8 mL) and Et3N (4 mL) at 0° C. was added TFAA (2.0 mL, 14 mmol) over 5 min. The reaction was warmed to rt and then stirred at this temperature for 2 h (complete by LCMS). The reaction solution was partitioned between water and CH2Cl2 and the organic phase was collected. The aqueous phase was further extracted with CH2Cl2. The organic layers were combined and washed with brine and dried over MgSO4. The solution was filtered and the solvent was removed in vacuo. The resulting material was redissolved in EtOAc and the product was precipitated via the addition of hexane. The solid material was collected by filtration and washed with cold hexanes and water to remove remaining Et3N. Isolated 580 mg (65%) of pure product as an off-white solid: LC/MS (ES) m/e 219 (M+H)+.

後処理

  1. customThe reaction solution was partitioned between water and CH2Cl2
  2. customthe organic phase was collected
  3. extractionThe aqueous phase was further extracted with CH2Cl2
  4. washwashed with brine
  5. dry with materialdried over MgSO4
  6. filtrationThe solution was filtered
  7. customthe solvent was removed in vacuo
  8. dissolutionThe resulting material was redissolved in EtOAc
  9. customthe product was precipitated via the addition of hexane
  10. filtrationThe solid material was collected by filtration
  11. washwashed with cold hexanes and water
  12. customto remove

出典と根拠

ORDレコード
ord-bd287612faf84cc19b4fe85cb646f832
出典データセット
uspto-grants-2010_04
特許番号
US07691850B2

反応ノート

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