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Ethanolamine → N-(2-Hydroxyethyl)-2-methyl-5-nitropyridine-3-carboxamide

HRID 972752
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인쇄 미리보기

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HRID 972752 반응식
[CH3:1][C:2]1[N:12]=[CH:11][C:10]([N+:13]([O-:15])=[O:14])=[CH:9][C:3]=1[C:4]([O:6]CC)=O.[NH2:16][CH2:17][CH2:18][OH:19]>C(O)C>[OH:19][CH2:18][CH2:17][NH:16][C:4](=[O:6])[C:3]1[CH:9]=[C:10]([N+:13]([O-:15])=[O:14])[CH:11]=[N:12][C:2]=1[CH3:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 700EthanolamineHCID 287239Ethyl 2-methyl-5-nitronicotinate

생성물 1

HCID 54034267N-(2-Hydroxyethyl)-2-methyl-5-nitropyridine-3-carboxamide

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of ethyl 2-methyl-5-nitronicotinate (1 g.) and 2-aminoethanol (4 ml.) in ethanol (5ml.) was stirred at room temperature for 16 hours. The solvent was distilled off, the residue was purified by silica gel chromatography and recrystallized from ethyl acetate n-hexane to give the desired yellow crystals. mp 144° - 145° C.

후처리

  1. distillationThe solvent was distilled off
  2. customthe residue was purified by silica gel chromatography
  3. customrecrystallized from ethyl acetate n-hexane
  4. customto give the desired yellow crystals

출처 및 근거

ORD 기록
ord-e50f24c5f5de465a89c287c68e8b8281
출처 데이터셋
uspto-grants-1977_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04053608

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