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Hydrochloric Acid → 3-fluoro-4-(2-phenyl-1H-pyrrolo[2,3-b]pyridin-4-yloxy)-phenylamine

HRID 1851094
ノート
印刷プレビュー

反応式

HRID 1851094 の反応式
C(OC(=O)[NH:7][C:8]1[CH:13]=[CH:12][C:11]([O:14][C:15]2[CH:20]=[CH:19][N:18]=[C:17]3[N:21](COCC[Si](C)(C)C)[C:22]([C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=4)=[CH:23][C:16]=23)=[C:10]([F:38])[CH:9]=1)(C)(C)C.Cl>CO>[F:38][C:10]1[CH:9]=[C:8]([NH2:7])[CH:13]=[CH:12][C:11]=1[O:14][C:15]1[CH:20]=[CH:19][N:18]=[C:17]2[NH:21][C:22]([C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)=[CH:23][C:16]=12
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 313Hydrochloric AcidHCID 583683903-fluoro-4-[2-phenyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrrolo[2,3-b]pyridin-4-yloxy]-phenyl-carbamic acid t-butyl ester

生成物 1

HCID 583683593-fluoro-4-(2-phenyl-1H-pyrrolo[2,3-b]pyridin-4-yloxy)-phenylamine収率 40%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

To a solution of 3-fluoro-4-[2-phenyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrrolo[2,3-b]pyridin-4-yloxy]-phenyl-carbamic acid t-butyl ester in methanol, a 1:1 solution (10 mL) of hydrochloric acid and methanol was added. The mixture was stirred at room temperature for 4 hours. The resulting reaction mixture was concentrated under reduced pressure and ether was added to the resulting residue. After stirring for 2 hours, the produced solid was collected by filtering. Thus obtained hydrochloride was dissolved in water and neutralized to about pH 8 by adding 1 M sodium hydroxide aqueous solution. The resulting mixture was extracted with ethyl acetate. The organic layer was separated and washed with sodium chloride aqueous solution. The organic layer was dried with Na2SO4 and then filtered. The filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (hexane:ethyl acetate=1:1) to give the target compound as a white solid (81 mg, 0.25 mmol, 40% yield).

後処理

  1. customThe resulting reaction mixture
  2. concentrationwas concentrated under reduced pressure and ether
  3. additionwas added to the resulting residue
  4. stirringAfter stirring for 2 hours
  5. customthe produced solid was collected
  6. filtrationby filtering
  7. dissolutionThus obtained hydrochloride was dissolved in water and neutralized to about pH 8
  8. additionby adding 1 M sodium hydroxide aqueous solution
  9. extractionThe resulting mixture was extracted with ethyl acetate
  10. customThe organic layer was separated
  11. washwashed with sodium chloride aqueous solution
  12. dry with materialThe organic layer was dried with Na2SO4
  13. filtrationfiltered
  14. concentrationThe filtrate was concentrated under reduced pressure
  15. customThe resulting residue was purified by silica gel chromatography (hexane:ethyl acetate=1:1)

出典と根拠

ORDレコード
ord-e5dbc61b7312445b85c8a27c4bc90c77
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08957102B2

反応ノート

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