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[5-(2-morpholin-4-yl-ethoxy)-1H-indol-2-yl]-methanol → 5-(2-morpholin-4-yl-ethoxy)-1H-indole-2-carbaldehyde

HRID 49051
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인쇄 미리보기

반응식

HRID 49051 반응식
[N:1]1([CH2:7][CH2:8][O:9][C:10]2[CH:11]=[C:12]3[C:16](=[CH:17][CH:18]=2)[NH:15][C:14]([CH2:19][OH:20])=[CH:13]3)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1>ClCCl.[O-2].[Mn+4].[O-2]>[N:1]1([CH2:7][CH2:8][O:9][C:10]2[CH:11]=[C:12]3[C:16](=[CH:17][CH:18]=2)[NH:15][C:14]([CH:19]=[O:20])=[CH:13]3)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1
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참가 물질

4

반응물 1

HCID 22042178[5-(2-morpholin-4-yl-ethoxy)-1H-indol-2-yl]-methanol

생성물 1

HCID 220421095-(2-morpholin-4-yl-ethoxy)-1H-indole-2-carbaldehyde수율 25.9%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 6344Dichloromethane용매

실험 절차

Manganese (IV) oxide (3.2 g, 36 mmol) was added to [5-(2-morpholin-4-yl-ethoxy)-1H-indol-2-yl]-methanol (0.7 g) in dichloromethane (150 mL). The mixture was stirred at room temperature for 16 hours. The precipitate was filtered off and the filtrate was concentrated. The residue was recrystallized from ethyl acetate and hexane to give 0.18 g of 5-(2-morpholin-4-yl-ethoxy)-1H-indole-2-carbaldehyde.

후처리

  1. filtrationThe precipitate was filtered off
  2. concentrationthe filtrate was concentrated
  3. customThe residue was recrystallized from ethyl acetate and hexane

출처 및 근거

ORD 기록
ord-227f1da4543844e396e9c64deb9089d5
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06706709B2

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