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Ethyl Acetate → 1-(4-methoxybenzyl)-1H-indazol-4-amine

HRID 2237410
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반응식

HRID 2237410 반응식
[CH3:1][O:2][C:3]1[CH:21]=[CH:20][C:6]([CH2:7][N:8]2[C:16]3[C:11](=[C:12]([N+:17]([O-])=O)[CH:13]=[CH:14][CH:15]=3)[CH:10]=[N:9]2)=[CH:5][CH:4]=1.C(OCC)(=O)C>C(O)C.[Pt](=O)=O>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:7][N:8]2[C:16]3[CH:15]=[CH:14][CH:13]=[C:12]([NH2:17])[C:11]=3[CH:10]=[N:9]2)=[CH:20][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 8857Ethyl AcetateHCID 685820841-(4-methoxybenzyl)-4-nitro-1H-indazole

생성물 1

HCID 685830011-(4-methoxybenzyl)-1H-indazol-4-amine수율 100%

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 702Ethanol용매

실험 절차

A suspension of 1-(4-methoxybenzyl)-4-nitro-1H-indazole (9 g, 31.77 mmol) and platinum(IV) oxide (0.433 g, 1.91 mmol) in ethanol (150 mL)/ethyl acetate (10 mL) was hydrogenated under 40 psi at 25° C. for 2 hours. The resulting mixture was filtered and the filtrate was concentrated to dryness to afford 1-(4-methoxybenzyl)-1H-indazol-4-amine (8.03 g, 100%) as a yellow-orange solid. Mass spectrum: MH+ 254.

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후처리

  1. filtrationThe resulting mixture was filtered
  2. concentrationthe filtrate was concentrated to dryness

출처 및 근거

ORD 기록
ord-f012f317e32a4e4baf04b166e474b40f
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07718653B2

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