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Thiourea → 5-(2-Methoxypyrimidin-5-ylmethyl)-2-thiouracil

HRID 705949
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인쇄 미리보기

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HRID 705949 반응식
O/[CH:2]=[C:3](/[CH2:8][C:9]1[CH:10]=[N:11][C:12]([O:15][CH3:16])=[N:13][CH:14]=1)\[C:4]([O:6]C)=O.[NH2:17][C:18]([NH2:20])=[S:19]>C(O)(C)C>[CH3:16][O:15][C:12]1[N:11]=[CH:10][C:9]([CH2:8][C:3]2[C:4](=[O:6])[NH:17][C:18](=[S:19])[NH:20][CH:2]=2)=[CH:14][N:13]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2723790ThioureaHCID 67773579(Z)-methyl 3-hydroxy-2-((2-methoxypyrimidin-5-yl)methyl)acrylate

생성물 1

HCID 219362445-(2-Methoxypyrimidin-5-ylmethyl)-2-thiouracil수율 39.8%

시약·촉매·용매 1

HCID 3776Isopropanol용매

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온도
83 °C

실험 절차

A mixture of (Z)-methyl 3-hydroxy-2-((2-methoxypyrimidin-5-yl)methyl)acrylate (10 g, 42.0 mmol) and thiourea (6.39 g, 84 mmol) in isopropanol (200 mL) was heated at 83° C. overnight. After removing the solvent, the residue was dissolved in water, washed with diethyl ether twice and acidified with AcOH to pH=4.5. The resulting solid was filtered and concentrated in vacuo to afford the title compound (4.4 g, 16.70 mmol, 39.8% yield) as yellow solid. LCMS: rt=1.31 min, [M+H+]=251

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후처리

  1. customAfter removing the solvent
  2. dissolutionthe residue was dissolved in water
  3. washwashed with diethyl ether twice
  4. filtrationThe resulting solid was filtered
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-7a50d8d531fb491e832717342fc0965f
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09174968B2

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