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

HRID 474608
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HRID 474608 반응식
O/[CH:2]=[C:3](/[CH2:9][C:10]1[CH:11]=[N:12][CH:13]=[N:14][CH:15]=1)\[C:4]([O:6]CC)=O.[NH2:16][C:17]([NH2:19])=[S:18].CC(C)([O-])C.[K+]>C(O)(C)C>[N:14]1[CH:15]=[C:10]([CH2:9][C:3]2[C:4](=[O:6])[NH:16][C:17](=[S:18])[NH:19][CH:2]=2)[CH:11]=[N:12][CH:13]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 2723790ThioureaHCID 23665647Potassium tert-butoxideHCID 60037935ethyl(2Z)-3-hydroxy-2-(5-pyrimidinylmethyl)-2-propenoate

생성물 1

HCID 109660395-(Pyrimid-5-ylmethyl)-2-thiouracil

시약·촉매·용매 1

HCID 3776Isopropanol용매

반응 조건

온도
80 °C

실험 절차

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

To a solution of ethyl (2Z)-3-hydroxy-2-(5-pyrimidinylmethyl)-2-propenoate (3 g, 7.20 mmol) in isopropanol (30 ml) was added thiourea (1.1 g, 14.45 mmol) and potassium tert-butoxide (1 g, 8.91 mmol). The mixture was heated at 80° C. for 4 h. The solvent was evaporated and residue was dissolved in water, extracted with ether twice to remove impurity. The aqueous phase was acidified to PH 4 with AcOH, and white participate formed. The mixture was filtered to afford the title compound as a white solid.

후처리

  1. customThe solvent was evaporated
  2. dissolutionresidue was dissolved in water
  3. extractionextracted with ether twice
  4. customto remove impurity
  5. customwhite participate formed
  6. filtrationThe mixture was filtered

출처 및 근거

ORD 기록
ord-0d224448ab5b46e2a50691e72cb7104b
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08637536B2

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