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6-Nitro-4-oxo-1-propionyl1,2,3,4-tetrahydroquinoline → 6-Amino-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline

HRID 35676
노트
인쇄 미리보기

반응식

HRID 35676 반응식
[N+:1]([C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[N:10]([C:14](=[O:17])[CH2:15][CH3:16])[CH2:9][CH2:8][C:7]2=[O:18])([O-])=O>CO.[Pd]>[NH2:1][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[N:10]([C:14](=[O:17])[CH2:15][CH3:16])[CH2:9][CH2:8][C:7]2=[O:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 212947876-Nitro-4-oxo-1-propionyl1,2,3,4-tetrahydroquinoline

생성물 1

HCID 212947846-Amino-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline수율 90.1%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

A solution of 6-nitro-4-oxo-1-propionyl1,2,3,4-tetrahydroquinoline (6.076 g) in methanol (60 ml) was hydrogenated over 5% palladium on carbon (0.5 g) under atmospheric pressure at ambient temperature. After the theoretical amount of hydrogen gas was absorbed, the catalyst was filtered off and the filtrate was evaporated in vacuo. The residual solid was washed with diethyl ether and dried to give 6amino-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline (4.815 g).

후처리

  1. customAfter the theoretical amount of hydrogen gas was absorbed
  2. filtrationthe catalyst was filtered off
  3. customthe filtrate was evaporated in vacuo
  4. washThe residual solid was washed with diethyl ether
  5. customdried

출처 및 근거

ORD 기록
ord-0af32720cf964cb6b5c302da4faf5314
출처 데이터셋
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04767780

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