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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 416749생성일: 2026년 10월 24일

Sodium Dithionite → HCID 178488875, 화합물

https://huagongshe.com/ko/reaction/416749

반응식

참여 물질

역할이름HCID투입량
반응물Sodium DithioniteHCID 24489—
반응물4-MethoxybenzaldehydeHCID 31244—
반응물5-Chloro-3-nitro-4-(4-(pyridin-4-ylmethyl)piperazin-1-yl)pyridin-2-amineHCID 46867129—
용매EthanolHCID 702—
생성물HCID 178488875HCID 178488875—

반응 조건

온도70 °C

반응 단계

To a mixture of 5-chloro-3-nitro-4-(4-(pyridin-4-ylmethyl)piperazin-1-yl)pyridin-2-amine (0.031 g, 0.09 mmol), and ethanol (3.0 ml) was added 4-methoxybenzaldehyde (0.020 g, 0.14 mmol) with the aid of ethanol (1 ml) followed by a freshly prepared aqueous solution of Na2S2O4 (1M; 0.36 ml, 0.36 mmol). The reaction mixture was heated at 70° C. for 5 h, then allowed to cool to room temperature and the solvents were removed in vacuo. The residue was triturated with water, and the precipitate was collected by filtration, washed with water, ethanol, and diethyl ether. This material was further purified on a 10 g isolute silica column using a gradient of methanol (0 to 5%) in ethyl acetate/dichloromethane (v/v; 1:1) as eluant. The title compound was obtained as a pale yellow solid (0.007 g, 18%); 1H-NMR (500 MHz, DMSO-d6) 2.61 (br s, 4H, piperazine N(CH2)2), 3.71 (br s, 4H, piperazine N(CH2)2), 3.61 (s, 2H, NCH2), 3.83 (s, 3H, OMe), 7.09 (d, J=8.85 Hz, 2H) and 8.12 (d, J=8.80 Hz, 2H) (3,5-C6H4OMe and 2,6-C6H4—OMe), 7.40 (d, J=5.86 Hz, 2H), and 8.54 (d, J=4.48 Hz, 2H) (pyrid-4-yl protons), 8.08 (s, 1H, imidazo[4,5-b]pyridine 5-H), 13.37 (s, 1H, imidazo[4,5-b]pyridine N—H);

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08088761B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-8ba95cbbad9e49bd811af91b1d2fe141
출처 메모uspto-grants-2012_01