Hydrochloric Acid → Methyl 4-(4-cyanophenyl)-6-methyl-2-thioxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydro-5-pyrimidinecarboxylate

HRID 570865

반응식

HRID 570865 반응식
[F:1][C:2]([F:14])([F:13])[C:3]1[CH:4]=[C:5]([NH:9][C:10]([NH2:12])=[S:11])[CH:6]=[CH:7][CH:8]=1.[C:15]([O:21][CH3:22])(=[O:20])[CH2:16][C:17]([CH3:19])=O.C[Si](OP([O-])([O-])=O)(C)C.Cl.[CH2:33]1[CH2:37]O[CH2:35][CH2:34]1>>[CH3:22][O:21][C:15]([C:16]1[CH:35]([C:34]2[CH:2]=[CH:3][C:4]([C:5]#[N:9])=[CH:37][CH:33]=2)[NH:12][C:10](=[S:11])[N:9]([C:5]2[CH:6]=[CH:7][CH:8]=[C:3]([C:2]([F:1])([F:13])[F:14])[CH:4]=2)[C:17]=1[CH3:19])=[O:20]

참가 물질

6

반응 조건

온도
70 °C

실험 절차

To a solution of 3-trifluoromethylphenylthiourea (2.2 g, 10 mmol) 4-cyanobenzaldehyde (1.4 g, 11 mmol) and methyl acetoacetate (1.2 mL, 11 mmol) in THF (40 mL) was added trimethylsilylphosphate (1.8 g) and the mixture heated at 70° C. After 17 hours, the reaction mixture was allowed to cool, then poured onto 0.5 M HCl (200 mL) and extracted into EtOAc. The organic phase was washed with water, then brine, dried (Na2SO4) and concentrated in vacuo. The resulting residue was purified by silica gel chromatography eluting with a gradient of 20-30% EtOAc in cyclohexane Appropriate fractions were combined and concentrated in vacuo to yield the title compound as a white foam (3.7 g).

후처리

  1. temperatureto cool
  2. extractionextracted into EtOAc
  3. washThe organic phase was washed with water
  4. dry with materialbrine, dried (Na2SO4)
  5. concentrationconcentrated in vacuo
  6. customThe resulting residue was purified by silica gel chromatography
  7. washeluting with a gradient of 20-30% EtOAc in cyclohexane Appropriate fractions
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-3578777d515d4a10b4fdb51e498dd236
출처 데이터셋
uspto-grants-2015_05
특허 번호
US09023855B2

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