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[5-(3-pyrrolidin-1-yl-propyl)-1H-indol-2-yl]-methanol → 5-(3-pyrrolidin-1-yl-propyl)-1H-indole-2-carbaldehyde

HRID 49060
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HRID 49060 반응식
[N:1]1([CH2:6][CH2:7][CH2:8][C:9]2[CH:10]=[C:11]3[C:15](=[CH:16][CH:17]=2)[NH:14][C:13]([CH2:18][OH:19])=[CH:12]3)[CH2:5][CH2:4][CH2:3][CH2:2]1>ClCCl.C1(C)C=CC=CC=1.[O-2].[Mn+4].[O-2]>[N:1]1([CH2:6][CH2:7][CH2:8][C:9]2[CH:10]=[C:11]3[C:15](=[CH:16][CH:17]=2)[NH:14][C:13]([CH:18]=[O:19])=[CH:12]3)[CH2:5][CH2:4][CH2:3][CH2:2]1
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참가 물질

5

반응물 1

HCID 22042173[5-(3-pyrrolidin-1-yl-propyl)-1H-indol-2-yl]-methanol

생성물 1

HCID 220421225-(3-pyrrolidin-1-yl-propyl)-1H-indole-2-carbaldehyde수율 72.6%

시약·촉매·용매 3

HCID 178418406HCID 178418406, 화합물촉매HCID 1140Toluene용매HCID 6344Dichloromethane용매

실험 절차

Manganese (IV) oxide (4.7 g, 54 mmol) was added to a mixture of [5-(3-pyrrolidin-1-yl-propyl)-1H-indol-2-yl]-methanol (940 mg, 3.6 mmol) in dichloromethane (150 mL) and toluene (150 mL). The mixture was stirred at room temperature for overnight. The reaction was filtered through a pad of celite and the filtrate was concentrated to give 670 mg (72%) of 5-(3-pyrrolidin-1-yl-propyl)-1H-indole-2-carbaldehyde.

후처리

  1. filtrationThe reaction was filtered through a pad of celite
  2. concentrationthe filtrate was concentrated

출처 및 근거

ORD 기록
ord-853f4baa99d24863b3a950a94c54b118
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06706709B2

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