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(4-(Ethylamino)-2-(methylthio)pyrimidin-5-yl)methanol → 4-(Ethylamino)-2-(methylthio)pyrimidine-5-carbaldehyde

HRID 3221
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인쇄 미리보기

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HRID 3221 반응식
[CH2:1]([NH:3][C:4]1[C:9]([CH2:10][OH:11])=[CH:8][N:7]=[C:6]([S:12][CH3:13])[N:5]=1)[CH3:2]>C(Cl)(Cl)Cl.[O-2].[Mn+2]>[CH2:1]([NH:3][C:4]1[C:9]([CH:10]=[O:11])=[CH:8][N:7]=[C:6]([S:12][CH3:13])[N:5]=1)[CH3:2]
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참가 물질

4

반응물 1

HCID 10584149(4-(Ethylamino)-2-(methylthio)pyrimidin-5-yl)methanol

생성물 1

HCID 107504444-(Ethylamino)-2-(methylthio)pyrimidine-5-carbaldehyde수율 97.8%

시약·촉매·용매 2

HCID 160959Manganese oxide촉매2회HCID 6212Chloroform용매

실험 절차

To 4-ethylamino-2-methylthio-5-pyrimidinemethanol (6.44 g, 32.4 mmol) in 600 mL of chloroform was added manganese oxide (21.0 g, 241 mmol) over 3 minutes. The suspension was stirred at room temperature for 2 hours, and an additional 5.5 g of manganese oxide was added. Stirring was continued for 4.5 hours. The mixture was then filtered through celite washing with chloroform. The filtrate was concentrated in vacuo to give 6.25 g (97%) of 4-ethylamino-2-methylthio-5-formylpyrimidine; mp 58°-61° C.

후처리

  1. stirringStirring
  2. waitwas continued for 4.5 hours
  3. filtrationThe mixture was then filtered
  4. washthrough celite washing with chloroform
  5. concentrationThe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-0f80dab124bd4936956f14f0363292fa
출처 데이터셋
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05733914

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