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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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(5-Methyl-6-methylaminopyridin-2-yl)methanol → 5-Methyl-6-methylamino-2-pyridinecarboxaldehyde

HRID 376301
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인쇄 미리보기

반응식

HRID 376301 반응식
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:10][OH:11])=[N:6][C:7]=1[NH:8][CH3:9]>C(Cl)(Cl)Cl.[O-2].[O-2].[Mn+4]>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([CH:10]=[O:11])=[N:6][C:7]=1[NH:8][CH3:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 10702001(5-Methyl-6-methylaminopyridin-2-yl)methanol

생성물 1

HCID 105348255-Methyl-6-methylamino-2-pyridinecarboxaldehyde

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 6212Chloroform용매

실험 절차

A suspension of 0.33 g of (5-methyl-6-methylaminopyridin-2-yl)methanol (2.17 mmol) and 1.6 g of manganese dioxide (18.4 mmol) in 12 ml of chloroform is heated under reflux for 1 hour. The insoluble matter is removed by filtration on celite and then the solvent evaporated under vacuum. The title product is purified by chromatography on a silica column (eluent: chloroform). 0.25 g of a yellow solid is recovered.

후처리

  1. temperatureis heated
  2. temperatureunder reflux for 1 hour
  3. customThe insoluble matter is removed by filtration on celite
  4. customthe solvent evaporated under vacuum
  5. customThe title product is purified by chromatography on a silica column (eluent: chloroform)
  6. custom0.25 g of a yellow solid is recovered

출처 및 근거

ORD 기록
ord-1478e1772b3e4ab19c1c736cf92f7273
출처 데이터셋
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06020345

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