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2-Hydrazinopyridine → HCID 178438380, 화합물

HRID 1911944
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HRID 1911944 반응식
[C:1]([CH:9]([CH2:15][CH2:16][CH3:17])[C:10]([O:12]CC)=O)(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH:18]([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][N:21]=1)[NH2:19]>C(O)C>[C:2]1([C:1]2[C:9]([CH2:15][CH2:16][CH3:17])=[C:10]([OH:12])[N:18]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][N:21]=3)[N:19]=2)[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 786452-HydrazinopyridineHCID 251321ethyl 2-benzoylpentanoate

생성물 1

HCID 178438380HCID 178438380, 화합물수율 80%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
100 °C

실험 절차

Ethyl 2-benzoylpentanoate (355 mg, 1.5 mmol) was dissolved in 5 mL of ethanol to which 2-hydrazinopyridine (163 mg, 1.5 mmol) was then added, followed by refluxing at 100° C. After 20 hours, ethanol was concentrated, followed by extraction with ethyl acetate. The extract was washed two or three times with water, and the organic layer was dried over anhydrous MgSO4 and then concentrated. The resulting residue was purified by column chromatography (n-hexane:EA=10:1) to afford the title compound.

후처리

  1. additionwas then added
  2. concentrationethanol was concentrated
  3. extractionfollowed by extraction with ethyl acetate
  4. washThe extract was washed two or three times with water
  5. dry with materialthe organic layer was dried over anhydrous MgSO4
  6. concentrationconcentrated
  7. customThe resulting residue was purified by column chromatography (n-hexane:EA=10:1)

출처 및 근거

ORD 기록
ord-57c9c853c6e34252b2b2815618590a54
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08604210B2

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