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HCID 69044992, 화합물 → HCID 69043464, 화합물

HRID 925073
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HRID 925073 반응식
[O:1]=[C:2]1[C:11]2[CH2:10][CH2:9][CH2:8][CH2:7][C:6]=2[C:5]([CH2:12][CH:13]2[CH2:18][N:17](C(OCC3C=CC=CC=3)=O)[CH2:16][CH2:15][N:14]2[C:29]([O:31][C:32]([CH3:35])([CH3:34])[CH3:33])=[O:30])=[N:4][NH:3]1>O1CCCC1.[Pd]>[O:1]=[C:2]1[C:11]2[CH2:10][CH2:9][CH2:8][CH2:7][C:6]=2[C:5]([CH2:12][CH:13]2[CH2:18][NH:17][CH2:16][CH2:15][N:14]2[C:29]([O:31][C:32]([CH3:35])([CH3:34])[CH3:33])=[O:30])=[N:4][NH:3]1
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참가 물질

4

반응물 1

HCID 69044992HCID 69044992, 화합물

생성물 1

HCID 69043464HCID 69043464, 화합물

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8028Tetrahydrofuran용매

실험 절차

A solution of EXAMPLE 257D (0.77 g, 1.6 mmol) in tetrahydrofuran (100 ml) was treated with 10% palladium on carbon (85 mg, 0.8 mmol) at room temperature under hydrogen (balloon) overnight. The catalyst was removed by filtration, and the filtrate was concentrated. The residue was purified by flash chromatography (0-15% gradient of methanol in CH2Cl2) to provide the title compound. MS (DCI/NH3) m/z 349 (M+H)+.

후처리

custom
The catalyst was removed by filtration
  • concentrationthe filtrate was concentrated
  • customThe residue was purified by flash chromatography (0-15% gradient of methanol in CH2Cl2)
  • 출처 및 근거

    ORD 기록
    ord-ad5886167b9448519c9c87b74b4fbe92
    출처 데이터셋
    uspto-grants-2016_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09283222B2

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