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6-(1H-Indol-4-yl)-1-methyl-4-nitro-1H-indazole → 6-(1H-Indol-4-yl)-1-methyl-1H-indazol-4-amine

HRID 1615978
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인쇄 미리보기

반응식

HRID 1615978 반응식
[NH:1]1[C:9]2[C:4](=[C:5]([C:10]3[CH:18]=[C:17]4[C:13]([CH:14]=[N:15][N:16]4[CH3:19])=[C:12]([N+:20]([O-])=O)[CH:11]=3)[CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1>C(OCC)(=O)C.[Pd]>[NH:1]1[C:9]2[C:4](=[C:5]([C:10]3[CH:11]=[C:12]([NH2:20])[C:13]4[CH:14]=[N:15][N:16]([CH3:19])[C:17]=4[CH:18]=3)[CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 582679906-(1H-Indol-4-yl)-1-methyl-4-nitro-1H-indazole

생성물 1

HCID 582680236-(1H-Indol-4-yl)-1-methyl-1H-indazol-4-amine수율 157%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8857Ethyl Acetate용매

실험 절차

6-(1H-Indol-4-yl)-1-methyl-4-nitro-1H-indazole (49 mg, 0.17 mmol) was dissolved in ethyl acetate (10 ml) and treated with 10% Pd/C (5 mg) then stirred under hydrogen for 2 h before stirring under nitrogen over the weekend. The reaction was filtered through a Celite cartridge, washing with ethyl acetate, then evaporated to dryness to give the title compound (70 mg) as a grey solid.

후처리

  1. stirringbefore stirring under nitrogen over the weekend
  2. filtrationThe reaction was filtered through a Celite cartridge
  3. washwashing with ethyl acetate
  4. customevaporated to dryness

출처 및 근거

ORD 기록
ord-a1d29d93a55e4fcc90747150e8e20905
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08765743B2

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