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tert-butyl 4-nitro-1H-indazole-1-carboxylate → tert-Butyl 4-amino-1H-indazole-1-carboxylate

HRID 2101676
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반응식

HRID 2101676 반응식
[N+:1]([C:4]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:5]=1[CH:6]=[N:7][N:8]2[C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])([O-])=O>C(O)C.[Pd]>[NH2:1][C:4]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:5]=1[CH:6]=[N:7][N:8]2[C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 59233580tert-butyl 4-nitro-1H-indazole-1-carboxylate

생성물 1

HCID 34176514tert-Butyl 4-amino-1H-indazole-1-carboxylate수율 96.9%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

1,1-Dimethylethyl 4-nitro-1H-indazole-1-carboxylate (1.2 g) was dissolved in ethanol (150 ml) and stirred with 10% palladium on carbon (0.24 g) under an atmosphere of hydrogen (1 atmosphere pressure) for 18 h. The solution was filtered through a pad of celite and the filtrate concentrated in vacuo to give the title compound as a yellow-orange solid (1.03 g).

후처리

  1. filtrationThe solution was filtered through a pad of celite
  2. concentrationthe filtrate concentrated in vacuo

출처 및 근거

ORD 기록
ord-ac0c81a5fe944f0f82b75a9faca18b61
출처 데이터셋
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07572915B2

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