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HCID 16739334, 화합물 → HCID 21099424, 화합물

HRID 2376979
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HRID 2376979 반응식
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1/[CH:9]=[CH:10]/[C:11]1[CH:16]=[CH:15][C:14]([S:17]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)(=[O:19])=[O:18])=[CH:13][CH:12]=1>C(OCC)(=O)C.[Pd]>[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[CH2:9][CH2:10][C:11]1[CH:16]=[CH:15][C:14]([S:17]([C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)(=[O:19])=[O:18])=[CH:13][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 16739334HCID 16739334, 화합물

생성물 1

HCID 21099424HCID 21099424, 화합물수율 40.1%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8857Ethyl Acetate용매

실험 절차

2,4-Difluoro-1-{(E)-2-[4-(phenylsulfonyl)phenyl]vinyl}benzene (Example 51, 57 mg, 0.16 mmol) and palladium (10% wt. on activated carbon, 20 mg) were combined in ethyl acetate (20 mL) and shaken in a Parr apparatus for 2 hours. The catalyst was removed by filtration and the filtrate evaporated in vacuo. The residue was purified by HPLC to yield the title compound as a white solid (23 mg, 40%). δH (400 z, CDCl3): 7.93-7.91 (2H, m), 7.84-7.82 (2H, m), 7.56-7.46 (3H, m), 7.27-7.24 (2H, m), 7.00-6.94 (1H, m), 6.76-6.70 (2H, m), 2.92-2.84 (4H, m).

후처리

  1. customThe catalyst was removed by filtration
  2. customthe filtrate evaporated in vacuo
  3. customThe residue was purified by HPLC

출처 및 근거

ORD 기록
ord-45e672d9392f480f927dce78e31dc8b7
출처 데이터셋
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07468393B2

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