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3-Aminopyridine → 8-(3-Pyridyl)-8-azaspiro[4,5]decan-7,9-dione

HRID 1105687
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반응식

HRID 1105687 반응식
[CH2:1]1[CH2:5][C:4]2([CH2:12][C:10](=[O:11])[O:9][C:7](=O)[CH2:6]2)[CH2:3][CH2:2]1.[NH2:13][C:14]1[CH:15]=[N:16][CH:17]=[CH:18][CH:19]=1>C1(C)C(C)=CC=CC=1>[N:16]1[CH:17]=[CH:18][CH:19]=[C:14]([N:13]2[C:7](=[O:9])[CH2:6][C:4]3([CH2:3][CH2:2][CH2:1][CH2:5]3)[CH2:12][C:10]2=[O:11])[CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 100093-AminopyridineHCID 79743Cyclopentane-1,1-diacetic anhydride

생성물 1

HCID 126505138-(3-Pyridyl)-8-azaspiro[4,5]decan-7,9-dione

시약·촉매·용매 1

HCID 7237O-Xylene용매

실험 절차

The starting material is prepared as follows. The mixture of 16.8 g of 3,3-tetramethyleneglutaric anhydride, 9.4 g of 3-aminopyridine and 225 ml of xylene is stirred and refluxed for 48 hours while collecting the water formed. After cooling in the refrigerator the precipitate obtained is filtered off and recrystallized from 300 ml ethanol-hexane, to yield the 8-(3-pyridyl)-8-azaspiro[4,5]decan-7,9-dione melting at 153°-154°.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • customThe starting material is prepared
  • temperaturerefluxed for 48 hours
  • customwhile collecting the water
  • customformed
  • temperatureAfter cooling in the refrigerator the precipitate
  • customobtained
  • filtrationis filtered off
  • customrecrystallized from 300 ml ethanol-hexane
  • 출처 및 근거

    ORD 기록
    ord-dc47ebac21da42e085fa5d17ea2c3d80
    출처 데이터셋
    uspto-grants-1982_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04309541

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