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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3-Benzyl-8-methyl-3,8-diazabicyclo[3.2.1]octane-2,4-dione → 3-Benzyl-3,8-diazabicyclo[3.2.1]octane-2,4-dione

HRID 1031574
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인쇄 미리보기

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HRID 1031574 반응식
Cl.N1C=CC=CC=1.[CH2:8]([N:15]1[C:21](=[O:22])[CH:20]2[N:23](C)[CH:17]([CH2:18][CH2:19]2)[C:16]1=[O:25])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1>O>[CH2:8]([N:15]1[C:16](=[O:25])[CH:17]2[NH:23][CH:20]([CH2:19][CH2:18]2)[C:21]1=[O:22])[C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=1
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참가 물질

4

반응물 2

HCID 2868213-Benzyl-8-methyl-3,8-diazabicyclo[3.2.1]octane-2,4-dioneHCID 10176127Pyridinium chloride

생성물 1

HCID 148395753-Benzyl-3,8-diazabicyclo[3.2.1]octane-2,4-dione수율 50%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

In a dry flask were mixed 15 g of dry pyridine hydrochloride and 3.15 g (130 mmol) of 3-benzyl-2,4-dioxo-8-methyl-3,8-diazabicyclo [3.2.1] octane prepared according to U.S. Pat. No. 3,328,398 in 1967, Jun. 27. The mixture was heated in an oil bath preheated at 220° C. for 20 mn, cooled in an ice-bath, dissolved in 90 ml water, extracted four times with 100 ml ethyl ether. The organic layers were collected and dried over magnesium sulfate. After removing the solvent, the residue was chromatographied over silica-gel using dichloromethane/ethylacetate (80:20) to afford 1.5 g of the title compound (50%). M.P. 72° C.

후처리

  1. customprepared
  2. temperatureThe mixture was heated in an oil bath
  3. custompreheated at 220° C. for 20 mn
  4. temperaturecooled in an ice-bath
  5. extractionextracted four times with 100 ml ethyl ether
  6. customThe organic layers were collected
  7. dry with materialdried over magnesium sulfate
  8. customAfter removing the solvent

출처 및 근거

ORD 기록
ord-51b4efaf71b94ff69d31680fde10eaa3
출처 데이터셋
uspto-grants-1990_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04954507

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