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Methyl 2-(6-(benzyloxy)-5-phenylpyridin-3-ylamino)-5-cyclopropylbenzoate → HCID 178524103、化合物

HRID 42056
ノート
印刷プレビュー

反応式

HRID 42056 の反応式
C([O:8][C:9]1[N:14]=[CH:13][C:12]([NH:15][C:16]2[CH:25]=[CH:24][C:23]([CH:26]3[CH2:28][CH2:27]3)=[CH:22][C:17]=2[C:18]([O:20]C)=[O:19])=[CH:11][C:10]=1[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)C1C=CC=CC=1>C(O)(C(F)(F)F)=O>[CH:26]1([C:23]2[CH:24]=[CH:25][C:16]([NH:15][C:12]3[CH:13]=[N:14][C:9]([OH:8])=[C:10]([C:29]4[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=4)[CH:11]=3)=[C:17]([CH:22]=2)[C:18]([OH:20])=[O:19])[CH2:27][CH2:28]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 1

HCID 67394538Methyl 2-(6-(benzyloxy)-5-phenylpyridin-3-ylamino)-5-cyclopropylbenzoate

生成物 1

HCID 178524103HCID 178524103、化合物

試薬・触媒・溶媒 1

HCID 6422Trifluoroacetic acid溶媒

実験手順

A solution of methyl 2-(6-(benzyloxy)-5-phenylpyridin-3-ylamino)-5-cyclopropylbenzoate (0.34 mmol, 0.155 g) in TFA (1.3 ml) was stirred at 45° C. for 30 minutes. The solvent was removed under reduced pressure. The crude mixture was solved in ethanol (2 ml), 2N aqueous NaOH were added and stirred at room temperature for 16 hours. The solvent was removed and the crude was neutralised with 2N aqueous HCl and extracted with CHCl3. The crude mixture was purified by ionic exchange through a SCX cartridge affording 0.060 g (50% of yield).

後処理

  1. customThe solvent was removed under reduced pressure
  • addition2N aqueous NaOH were added
  • customThe solvent was removed
  • extractionextracted with CHCl3
  • customThe crude mixture was purified by ionic exchange through a SCX cartridge
  • customaffording
  • custom0.060 g (50% of yield)
  • 出典と根拠

    ORDレコード
    ord-c915df7c41ed40f79bf84532c54bfa1a
    出典データセット
    uspto-grants-2013_09
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US08536165B2

    反応ノート

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