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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 15677249, 화합물 → HCID 178440053, 화합물

HRID 1462218
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HRID 1462218 반응식
[N:1](=[C:3]([C:7](=[O:9])[CH3:8])[C:4](=O)[CH3:5])O.C[NH:11][CH:12](C(O)=O)[CH2:13][CH2:14][CH3:15]>C(#N)C>[C:7]([C:3]1[NH:1][C:12]([CH2:13][CH2:14][CH3:15])=[N:11][C:4]=1[CH3:5])(=[O:9])[CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 15677249HCID 15677249, 화합물HCID 178468373HCID 178468373, 화합물

생성물 1

HCID 178440053HCID 178440053, 화합물수율 51.6%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To 40 g (0.31 moles) of 3-oximino-2,4-pentanedione dissolved in 297 ml of acetonitrile was added 40.64 g (0.31 moles) of methyl d,1-norvaline. The reaction mixture was refluxed 21.2 h under nitrogen, cooled, then concentrated in vacuo. The resulting oil was dissolved in 50 ml of ethanol and 140 ml of 10% aqueous sodium hydroxide. After 4 h of reflux, the cooled mixture was extracted with ethyl acetate (900 ml total) and dried over anhydrous sodium sulfate. Removal of the solvent in vacuo afforded 0.16 moles (51% yield) of 5-acetyl-4-methyl-2-propylimidazole.

후처리

  1. temperatureThe reaction mixture was refluxed 21.2 h under nitrogen
  2. temperaturecooled
  3. concentrationconcentrated in vacuo
  4. dissolutionThe resulting oil was dissolved in 50 ml of ethanol
  5. temperatureAfter 4 h of reflux
  6. extractionthe cooled mixture was extracted with ethyl acetate (900 ml total)
  7. dry with materialdried over anhydrous sodium sulfate
  8. customRemoval of the solvent in vacuo

출처 및 근거

ORD 기록
ord-742f854ecb9944b6b84046f18d861a41
출처 데이터셋
uspto-grants-1984_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04459413

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