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Thioacetamide → Ethyl 2-methyl-5-(1-methylethyl)-1,3-thiazole-4-carboxylate

HRID 244624
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HRID 244624 반응식
[C:1]([NH2:4])(=[S:3])[CH3:2].Br[CH:6]([CH:14]([CH3:16])[CH3:15])[C:7](=O)[C:8]([O:10][CH2:11][CH3:12])=[O:9]>C(O)C>[CH3:2][C:1]1[S:3][C:6]([CH:14]([CH3:16])[CH3:15])=[C:7]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[N:4]=1
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참가 물질

4

반응물 2

HCID 2723949ThioacetamideHCID 58356425Ethyl 3-bromo-4-methyl-2-oxopentanoate

생성물 1

HCID 58356351Ethyl 2-methyl-5-(1-methylethyl)-1,3-thiazole-4-carboxylate수율 62.4%

시약·촉매·용매 1

HCID 702Ethanol용매2회

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온도
80 °C

실험 절차

To a solution of thioacetamide (158 mg) in ethanol (20 ml) was added ethyl 3-bromo-4-methyl-2-oxopentanoate (500 mg) in ethanol (0.5 ml). Molecular sieves (100 mg) were added and the mixture was heated at 80° C. for 18 h. The mixture was filtered, washing with ethanol (5 ml) and the solvent removed in vacuo. The residue triturated with DCM and the solid removed by filtration. The filtrate was concentrated to ˜5 ml and purified by column chromatography on silica gel (10 g silica), eluting with a gradient of 0-100% ethyl acetate in cyclohexane to give the title compound as a yellow oil (280 mg).

후처리

  1. additionMolecular sieves (100 mg) were added
  2. filtrationThe mixture was filtered
  3. washwashing with ethanol (5 ml)
  4. customthe solvent removed in vacuo
  5. customThe residue triturated with DCM
  6. customthe solid removed by filtration
  7. concentrationThe filtrate was concentrated to ˜5 ml
  8. custompurified by column chromatography on silica gel (10 g silica)
  9. washeluting with a gradient of 0-100% ethyl acetate in cyclohexane

출처 및 근거

ORD 기록
ord-6e39d18be1de4aca94da424273dadef3
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658635B2

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