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Sodium hydride → HCID 57422597, 화합물

HRID 2426775
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HRID 2426775 반응식
[H-].[Na+].[Br:3][C:4]1[C:5]([CH3:11])=[CH:6][C:7]([OH:10])=[N:8][CH:9]=1.CC1C=CC(S(O[CH2:23][CH2:24][C:25]([OH:28])([CH3:27])[CH3:26])(=O)=O)=CC=1>CN(C=O)C>[Br:3][C:4]1[C:5]([CH3:11])=[CH:6][C:7]([O:10][CH2:23][CH2:24][C:25]([CH3:27])([OH:28])[CH3:26])=[N:8][CH:9]=1.[Br:3][C:4]1[C:5]([CH3:11])=[CH:6][C:7](=[O:10])[N:8]([CH2:23][CH2:24][C:25]([OH:28])([CH3:27])[CH3:26])[CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 24758Sodium hydrideHCID 140012952-Methyl-4-[(4-methylbenzenesulfonyl)oxy]butan-2-olHCID 178429280HCID 178429280, 화합물

생성물 2

HCID 57422597HCID 57422597, 화합물HCID 574225985-bromo-1-(3-hydroxy-3-methylbutyl)-4-methylpyridin-2(1H)-one

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

실험 절차

In an atmosphere of nitrogen, sodium hydride was added under ice-cooling to a mixture of 5-bromo-4-methylpyridin-2-ol and DMF, followed by stirring at room temperature for 1 hour. Then, 3-hydroxy-3-methylbutyl 4-methylbenzenesulfonate was added thereto, followed by stirring at 40° C. for 14 hours to obtain 4-[(5-bromo-4-methylpyridin-2-yl)oxy]2-methylbutan-2-ol and 5-bromo-1-(3-hydroxy-3-methylbutyl)-4-methylpyridin-2(1H)-one.

후처리

  1. stirringby stirring at 40° C. for 14 hours

출처 및 근거

ORD 기록
ord-c2916366ee204a46a7cc614a309bdfab
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07968552B2

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