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1-(Azetidin-1-yl)-2-[4-(benzyloxy)-2-chlorophenyl]ethanone → 1-(Azetidin-1-yl)-2-(2-chloro-4-hydroxyphenyl)ethanone

HRID 1850722
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인쇄 미리보기

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HRID 1850722 반응식
[N:1]1([C:5](=[O:22])[CH2:6][C:7]2[CH:12]=[CH:11][C:10]([O:13]CC3C=CC=CC=3)=[CH:9][C:8]=2[Cl:21])[CH2:4][CH2:3][CH2:2]1>C(O)C.[OH-].[OH-].[Pd+2]>[N:1]1([C:5](=[O:22])[CH2:6][C:7]2[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][C:8]=2[Cl:21])[CH2:4][CH2:3][CH2:2]1
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참가 물질

4

반응물 1

HCID 867111801-(Azetidin-1-yl)-2-[4-(benzyloxy)-2-chlorophenyl]ethanone

생성물 1

HCID 708188251-(Azetidin-1-yl)-2-(2-chloro-4-hydroxyphenyl)ethanone

시약·촉매·용매 2

HCID 9942167Palladium hydroxide촉매HCID 702Ethanol용매

실험 절차

1-(azetidin-1-yl)-2-[4-(benzyloxy)-2-chlorophenyl]ethanone (520 mg, 1.65 mmol) was dissolved in ethanol (2 ml). and palladium hydroxide on carbon (20%) (116 mg, 0.165 mmol) added. The mixture was stirred under an atmosphere of hydrogen gas at RT overnight. The mixture was filtered and the filtrate concentrated under reduced pressure. The reside was purified by column chromatography using a Biotage RP C18 cartridge (30 g) using a gradient eluant of 10-100% water:acetonitrile+0.05% formic acid. to afford the title compound. LC/MS (m/z): 226 (M+H)+.

후처리

  1. filtrationThe mixture was filtered
  2. concentrationthe filtrate concentrated under reduced pressure
  3. customThe reside was purified by column chromatography

출처 및 근거

ORD 기록
ord-74805dda50fe4ecc90ab9c62c3320feb
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08957062B2

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