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Trimethylsilyldiazomethane → 2-(3-Methoxycarbonyl-phenyl)-4-oxo-1,3,8-triaza-spiro[4.5]dec-1-ene-8-carboxylic acid tert-butyl ester

HRID 1754923
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HRID 1754923 반응식
[CH3:1][Si](C=[N+]=[N-])(C)C.[C:8]([O:12][C:13]([N:15]1[CH2:34][CH2:33][C:18]2([N:22]=[C:21]([C:23]3[CH:28]=[CH:27][CH:26]=[C:25]([C:29]([OH:31])=[O:30])[CH:24]=3)[NH:20][C:19]2=[O:32])[CH2:17][CH2:16]1)=[O:14])([CH3:11])([CH3:10])[CH3:9]>CO>[C:8]([O:12][C:13]([N:15]1[CH2:16][CH2:17][C:18]2([N:22]=[C:21]([C:23]3[CH:28]=[CH:27][CH:26]=[C:25]([C:29]([O:31][CH3:1])=[O:30])[CH:24]=3)[NH:20][C:19]2=[O:32])[CH2:33][CH2:34]1)=[O:14])([CH3:11])([CH3:9])[CH3:10]
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참가 물질

4

반응물 2

HCID 167693Trimethylsilyldiazomethane2회HCID 66818237HCID 66818237, 화합물

생성물 1

HCID 668184592-(3-Methoxycarbonyl-phenyl)-4-oxo-1,3,8-triaza-spiro[4.5]dec-1-ene-8-carboxylic acid tert-butyl ester수율 44%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

(Trimethylsilyl)diazomethane (2.0 M in hexane, 4.0 ml, 8.0 mmol) was added dropwise to a solution of 2-(3-carboxy-phenyl)-4-oxo-1,3,8-triaza-spiro[4.5]dec-1-ene-8-carboxylic acid tert-butyl ester (200 mg, 0.54 mmol) in methanol (10 ml). The mixture was stirred at room temperature for one hour, and (trimethylsilyl)diazomethane (1.0 ml, 2.0 mmol) was then further added, followed by stirring for one hour. The reaction mixture was concentrated under reduced pressure, and the resulting solid was then washed with a solution of hexane/ethyl acetate=5/1 to give 2-(3-methoxycarbonyl-phenyl)-4-oxo-1,3,8-triaza-spiro[4.5]dec-1-ene-8-carboxylic acid tert-butyl ester (91.5 mg, 44%).

후처리

  1. stirringby stirring for one hour
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. washthe resulting solid was then washed with a solution of hexane/ethyl acetate=5/1

출처 및 근거

ORD 기록
ord-eded67fe921944f89f485755cfd6f155
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09169254B2

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