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HCID 68840871, 화합물 → HCID 68844805, 화합물

HRID 1889283
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반응식

HRID 1889283 반응식
[CH3:1][O:2][C:3](=[O:30])[C:4]([CH3:29])([NH:6][C:7]([C:9]1[CH:18]=[CH:17][C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[C:10]=1[C:19]#[C:20][CH2:21][CH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)=[O:8])[CH3:5]>CO.[Pd]>[CH3:1][O:2][C:3](=[O:30])[C:4]([CH3:5])([NH:6][C:7]([C:9]1[CH:18]=[CH:17][C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[C:10]=1[CH2:19][CH2:20][CH2:21][CH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)=[O:8])[CH3:29]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 68840871HCID 68840871, 화합물

생성물 1

HCID 68844805HCID 68844805, 화합물수율 95%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

50 mg of 2-methyl-2-{[1-(4-phenyl-but-1-ynyl)-naphthalene-2-carbonyl]-amino}-propionic acid methyl ester were dissolved in 5 ml methanol, and after addition of 10 mg of Pd/C (10%) hydrogenated for 6 h. The reaction was then filtrated and the filtrate was concentrated to yield 48 mg of 2-methyl-2-{[1-(4-phenyl-butyl)-naphthalene-2-carbonyl]-amino}-propionic acid methyl ester.

후처리

  • filtrationThe reaction was then filtrated
  • concentrationthe filtrate was concentrated
  • 출처 및 근거

    ORD 기록
    ord-fffbd8c336d243c3b1acc2ac55279c1f
    출처 데이터셋
    uspto-grants-2013_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08501981B2

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