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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 87180103, 화합물 → Ethyl 2-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate

HRID 1406403
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HRID 1406403 반응식
C([O:3][C:4](=O)/[CH:5]=[CH:6]/[C:7](=[C:13](/[NH2:15])\[CH3:14])/[C:8]([O:10][CH2:11][CH3:12])=[O:9])C>CN(C)C=O>[CH2:11]([O:10][C:8]([C:7]1[CH:6]=[CH:5][C:4](=[O:3])[NH:15][C:13]=1[CH3:14])=[O:9])[CH3:12]
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참가 물질

3

반응물 1

HCID 87180103HCID 87180103, 화합물2회

생성물 1

HCID 3299500Ethyl 2-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A solution of intermediate (5a), (E)-4-[1-amino-eth-(Z)-ylidene]-pent-2-enedioic acid diethyl ester (51 g, 225 mmol) in N,N-dimethylformamide (250 mL) was heated at 175° C. for 24 hours to give a dark brown solution. The resulting solution was allowed to cool and a pale brown precipitate slowly formed. The precipitate was removed by filtration and the solids washed with dichloromethane (75 mL) and hexane (100 mL) to give a pale yellow powder. The solids were dried in vacuo (60° C.) to give the title compound as a pale yellow powder, 14.45 g (36%)

후처리

  1. customto give a dark brown solution
  2. temperatureto cool
  3. customa pale brown precipitate slowly formed
  4. customThe precipitate was removed by filtration
  5. washthe solids washed with dichloromethane (75 mL) and hexane (100 mL)
  6. customto give a pale yellow powder
  7. customThe solids were dried in vacuo (60° C.)

출처 및 근거

ORD 기록
ord-155454a047d541128ed8cdb61e4cad88
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08916591B2

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