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HRID 1518531생성일: 2026년 10월 26일

4-Methoxybenzylamine → N-(4-methoxybenzyl)-5-bromo-3-(5-(2,3-dichlorophenyl)thiazol-4-yl)pyridin-2-amine

https://huagongshe.com/reaction/1518531

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참여 물질

역할이름HCID투입량
반응물4-MethoxybenzylamineHCID 75452—
반응물5-Bromo-2-chloro-3-(5-(2,3-dichlorophenyl)thiazol-4-yl)pyridineHCID 58180075—
용매1,2-DimethoxyethaneHCID 8071—
생성물N-(4-methoxybenzyl)-5-bromo-3-(5-(2,3-dichlorophenyl)thiazol-4-yl)pyridin-2-amineHCID 5817956585%

반응 단계

A solution of 5-bromo-2-chloro-3-(5-(2,3-dichlorophenyl)thiazol-4-yl)pyridine (520 mg, 1.24 mmol) and p-methoxybenzyl amine (373 mg, 2.72 mmol) in DME (12 mL) was stirred at 80° C. for 48 hours. The reaction mixture was concentrated and the residue purified by silica gel chromatography (0-25% EtOAc/hexanes) to give N-(4-methoxybenzyl)-5-bromo-3-(5-(2,3-dichlorophenyl)thiazol-4-yl)pyridin-2-amine as a pale yellow solid [631 mg, 85% yield; LC-MS, M+H=519.9; 1H-NMR (300 MHz, CDCl3) 8.85 (1 H, s), 8.00 (1 H, d, J=2.3 Hz), 7.45 (1H, dd, J=1.9, 7.6 Hz), 7.10-7.17 (4 H, m), 7.01 (1 H, d, J=2.4 Hz), 6.77 (1 H, t, J=6.7 Hz)].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08232406B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-c5fc8f3308ad4bcf9841ee0350f343a3
출처 메모uspto-grants-2012_07