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HCID 178418361, 화합물 → HCID 178481327, 화합물

HRID 2198546
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HRID 2198546 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([NH:10][NH:11][C:12]([N:14]([CH3:27])[C:15]2[CH:23]=[CH:22][CH:21]=[C:20]3[C:16]=2[C:17](=[O:26])[N:18]([CH3:25])[C:19]3=[O:24])=[O:13])=[CH:6][CH:5]=1)([O-])=O.[H][H]>O1CCCC1.[Pd]>[NH2:1][C:4]1[CH:9]=[CH:8][C:7]([NH:10][NH:11][C:12]([N:14]([CH3:27])[C:15]2[CH:23]=[CH:22][CH:21]=[C:20]3[C:16]=2[C:17](=[O:26])[N:18]([CH3:25])[C:19]3=[O:24])=[O:13])=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 178418361HCID 178418361, 화합물HCID 178481328HCID 178481328, 화합물

생성물 1

HCID 178481327HCID 178481327, 화합물수율 87%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8028Tetrahydrofuran용매

실험 절차

1-p-Nitrophenyl-4-methyl-4-(2-methyl-1,3-dioxoisoindolin-4-yl)semicarbazide (2.6 g) was dissolved in 300 ml tetrahydrofuran and a catalytic amount (about 200 mg) of 10% palladium on carbon was added. The mixture was hydrogenated on a Parr hydrogenation apparatus overnight at 40 psi hydrogen pressure. The mixture was filtered and the solvent was evaporated to give 2.0 g (87% yield).

후처리

  1. filtrationThe mixture was filtered
  2. customthe solvent was evaporated
  3. customto give 2.0 g (87% yield)

출처 및 근거

ORD 기록
ord-4a837dd057544051873c65ff1bf278be
출처 데이터셋
uspto-grants-1982_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04358525

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