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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-Benzyl-4-nitroisoindoline → Isoindolin-4-amine

HRID 1494826
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HRID 1494826 반응식
C([N:8]1[CH2:16][C:15]2[C:10](=[CH:11][CH:12]=[CH:13][C:14]=2[N+:17]([O-])=O)[CH2:9]1)C1C=CC=CC=1>CO.[Pd]>[NH2:17][C:14]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:15]=1[CH2:16][NH:8][CH2:9]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 147958602-Benzyl-4-nitroisoindoline

생성물 1

HCID 14795861Isoindolin-4-amine수율 61.6%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

11.5 g of 2-benzyl-4-nitroisoindoline was dissolved in 150 ml of methanol and to the solution was added 1.5 g of 10% palladium on carbon. The mixture was stirred under a hydrogen gas stream under atmospheric pressure for one day at room temperature and for another 5 days at 40° C.. The catalyst was removed by filtration and the filtrate was concentrated. The residue was purified by a vacuum distillation (bath temperature: 150°-180° C., pressure: 0.1 mmHg) to obtain 3.74 g of 4-aminoisoindoline.

후처리

  1. waitfor another 5 days at 40° C.
  2. customThe catalyst was removed by filtration
  3. concentrationthe filtrate was concentrated
  4. distillationThe residue was purified by a vacuum distillation (bath temperature: 150°-180° C., pressure: 0.1 mmHg)

출처 및 근거

ORD 기록
ord-044d71713e844378a4a53ff6ebfbc9cd
출처 데이터셋
uspto-grants-1991_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05026856

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