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Methyl 2-(6-(benzyloxy)-5-phenylpyridin-3-ylamino)-5-cyclopropylbenzoate → HCID 178524103, 화합물

HRID 42056
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HRID 42056 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

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

생성물 1

HCID 178524103HCID 178524103, 화합물

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

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).

후처리

  1. custom
The 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)
  • 출처 및 근거

    ORD 기록
    ord-c915df7c41ed40f79bf84532c54bfa1a
    출처 데이터셋
    uspto-grants-2013_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08536165B2

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