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5-(4-Phthalimidobut-1-yn-1-yl)-2'-deoxvuridine → 5-(4-Phthalimidobut-1-yl)-2'-deoxyuridine

HRID 1457512
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인쇄 미리보기

반응식

HRID 1457512 반응식
[C:1]1(=[O:31])[N:5]([CH2:6][CH2:7][C:8]#[C:9][C:10]2[C:11](=[O:25])[NH:12][C:13](=[O:24])[N:14]([CH:23]=2)[C@@H:15]2[O:22][C@H:19]([CH2:20][OH:21])[C@@H:17]([OH:18])[CH2:16]2)[C:4](=[O:26])[C:3]2=[CH:27][CH:28]=[CH:29][CH:30]=[C:2]12>CCO.[Ni]>[C:4]1(=[O:26])[N:5]([CH2:6][CH2:7][CH2:8][CH2:9][C:10]2[C:11](=[O:25])[NH:12][C:13](=[O:24])[N:14]([CH:23]=2)[C@@H:15]2[O:22][C@H:19]([CH2:20][OH:21])[C@@H:17]([OH:18])[CH2:16]2)[C:1](=[O:31])[C:2]2=[CH:30][CH:29]=[CH:28][CH:27]=[C:3]12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 543516515-(4-Phthalimidobut-1-yn-1-yl)-2'-deoxvuridine

생성물 1

HCID 543075585-(4-Phthalimidobut-1-yl)-2'-deoxyuridine수율 97%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 702Ethanol용매

실험 절차

1.00 Gram of 5-(4-Phthalimidobut-1-yn-1-yl)-2'-deoxyuridine was dissolved in 95% EtOH and about 3 g of neutral Raney nickel was added. After 48 hours, the catalyst was removed by cautious filtration and the filtrate was evaporated to a solid which was recrystallized from methanol-water to give 960 mg (97%) of the title compound.

후처리

  1. customthe catalyst was removed by cautious filtration
  2. customthe filtrate was evaporated to a solid which
  3. customwas recrystallized from methanol-water

출처 및 근거

ORD 기록
ord-86214e520a5746bcaf3082027d8f69fa
출처 데이터셋
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05849482

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