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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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5-(1-Methyl-propenyl)-pyridin-2-ylamine → 5-Sec-butyl-pyridin-2-ylamine

HRID 1920728
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HRID 1920728 반응식
[CH3:1][C:2]([C:5]1[CH:6]=[CH:7][C:8]([NH2:11])=[N:9][CH:10]=1)=[CH:3][CH3:4]>C(O)C.[Pd]>[CH:2]([C:5]1[CH:6]=[CH:7][C:8]([NH2:11])=[N:9][CH:10]=1)([CH2:3][CH3:4])[CH3:1]
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참가 물질

4

반응물 1

HCID 674932645-(1-Methyl-propenyl)-pyridin-2-ylamine

생성물 1

HCID 206746695-Sec-butyl-pyridin-2-ylamine수율 68.9%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A solution of 130 mg (0.87 mmol) of 5-(1-methyl-propenyl)-pyridin-2-ylamine in ethanol (5 mL) was reduced over palladium on charcoal (10 wt %, 13 mg) under a hydrogen atmosphere at room temperature for 18 h. The catalyst was separated by filtration through Celite® and washed with ethanol (5 mL). The filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (silica, eluent ethyl acetate) to afford 90 mg of 5-sec-butyl-pyridin-2-ylamine. ES−MS: m/z 151 [M+H+];

후처리

  1. customThe catalyst was separated by filtration through Celite®
  2. washwashed with ethanol (5 mL)
  3. concentrationThe filtrate was concentrated under reduced pressure
  4. customThe residue was purified by column chromatography (silica, eluent ethyl acetate)

출처 및 근거

ORD 기록
ord-32c8816a16184fce9443a6da2dc64478
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08173638B2

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