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HRID 401259생성일: 2026년 10월 24일

6-Nitro-1H-indole-3-carbonitrile → 6-amino-1H-indole-3-carbonitrile

https://huagongshe.com/ko/reaction/401259

반응식

참여 물질

역할이름HCID투입량
반응물6-Nitro-1H-indole-3-carbonitrileHCID 283179—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물6-amino-1H-indole-3-carbonitrileHCID 4441046499%

반응 단계

A suspension of 6-nitro-1H-indole-3-carbonitrile (4.6 g, 24.6 mmol) and 10% Pd—C (0.46 g) in EtOH (50 mL) was stirred under H2 (1 atm) at room temperature overnight. After filtration, the filtrate was concentrated and the residue was purified by column chromatography (Pet. Ether/EtOAc=3/1) to give 6-amino-1H-indole-3-carbonitrile (B-8) (1 g, 99%) as a pink powder. 1H NMR (DMSO-d6) δ 11.51 (s, 1H), 7.84 (d, J=2.4 Hz, 1H), 7.22 (d, J=8.4 Hz, 1H), 6.62 (s, 1H), 6.56 (d, J=8.4 Hz, 1H), 5.0 (s, 2H); ESI-MS 157.1 m/z (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741925B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-44dbff0632634a93b7eafa96004e5cef
출처 메모uspto-grants-2014_06