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[2-(Pyridin-2-yl)-1,3-thiazol-4-yl]methanol → 2-(Pyridin-2-yl)-1,3-thiazole-4-carbaldehyde

HRID 1682428
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HRID 1682428 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[S:8][CH:9]=[C:10]([CH2:12][OH:13])[N:11]=1>C1(C)C=CC=CC=1.[O-2].[Mn+2]>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[S:8][CH:9]=[C:10]([CH:12]=[O:13])[N:11]=1
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참가 물질

4

반응물 1

HCID 10750266[2-(Pyridin-2-yl)-1,3-thiazol-4-yl]methanol

생성물 1

HCID 21253372-(Pyridin-2-yl)-1,3-thiazole-4-carbaldehyde수율 87.1%

시약·촉매·용매 2

HCID 160959Manganese oxide촉매HCID 1140Toluene용매

실험 절차

5.8 g of the product of Stage D in 60 ml of toluene were refluxed for 2 hours in the presence of 13 g of manganese oxide and filtration was carried out. The solvent was evaporated under reduced pressure to obtain 5 g of the expected product melting at 131° C.

후처리

  1. customThe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-1199fb9f238f42b4b478dfad89ac424b
출처 데이터셋
uspto-grants-1997_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05635485

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