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Methyl p-toluenesulfonate → 5-Benzyl-7-methoxy-5-azaspiro[2.4]heptane

HRID 1010801
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HRID 1010801 반응식
[CH2:1]([N:8]1[CH2:14][CH:13]([OH:15])[C:10]2([CH2:12][CH2:11]2)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Na+].S(OC)([C:21]1C=CC(C)=CC=1)(=O)=O>CN(C=O)C>[CH2:1]([N:8]1[CH2:14][CH:13]([O:15][CH3:21])[C:10]2([CH2:11][CH2:12]2)[CH2:9]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
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참가 물질

5

반응물 3

HCID 6645Methyl p-toluenesulfonateHCID 24758Sodium hydrideHCID 584529235-Benzyl-5-azaspiro[2.4]heptan-7-ol

생성물 1

HCID 167382885-Benzyl-7-methoxy-5-azaspiro[2.4]heptane

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
0 °C

실험 절차

5-Benzyl-5-azaspiro[2.4]heptan-7-ol (200 mg) was dissolved into DMF (4 ml) and cooled at 0° C. NaH (120 mg) was added to the reaction and stirred for 10 minutes. To the reaction was added TsOMe (200 mg), the solution was heated at 80° C. for two hours. The reaction was quenched with water and extracted with EtOAc followed by washing with water, then brine and dried over Na2SO4 and evaporated to give the titled product. Mass: (M+1), 158

후처리

  1. temperaturethe solution was heated at 80° C. for two hours
  2. customThe reaction was quenched with water
  3. extractionextracted with EtOAc
  4. washby washing with water
  5. dry with materialbrine and dried over Na2SO4
  6. customevaporated

출처 및 근거

ORD 기록
ord-f54aada8aa714135bf3a53651debd1bd
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07977346B2

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