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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1040749생성일: 2026년 10월 24일

Potassium Iodide → N-[2-(7-Methoxy-8-nitro-1,2,4,5-tetrahydro-benzo[d]azepin-3-yl)-ethyl]-acetamide

https://huagongshe.com/ko/reaction/1040749

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물N-(2-Chloroethyl)acetamideHCID 81815—
반응물7-Methoxy-8-nitro-2,3,4,5-tetrahydro-1H-benzo[d]azepineHCID 67264351—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물N-[2-(7-Methoxy-8-nitro-1,2,4,5-tetrahydro-benzo[d]azepin-3-yl)-ethyl]-acetamideHCID 6726461515%

반응 단계

Into a 1-neck round-bottom flask was added 7-methoxy-8-nitro-2,3,4,5-tetrahydro-1H-benzo[d]azepine (0.5 g, 2.20 mmol), N-(2-chloro-ethyl)-acetamide (0.45 mL, 4.41 mmol), potassium iodide (92 mg, 0.55 mmol), and potassium carbonate (900 mg, 7 mmol), in N-methylpyrrolidinone (5 mL), and the reaction was heated at 90 overnight. The reaction mixture was next partitioned between water and ethyl acetate, and the layers separated. The aqueous phase was extracted twice with ethyl acetate and the combined organic extracts were washed with water, dried (MgSO4), filtered, and concentrated, and the product was isolated by flash chromatography on SiO2 (MeOH/dichloromethane 0-20%) to give N-[2-(7-Methoxy-8-nitro-1,2,4,5-tetrahydro-benzo[d]azepin-3-yl)-ethyl]-acetamide (100 mg, 15%). 1H-NMR (CDCl3) δ 7.67 (s, 1H), 6.84 (s, 1H), 6.11 (br s, 1H), 3.94 (s, 3H), 3.38 (m, 2H), 2.95 (m, 2H), 2.89 (m, 2H), 2.66 (m, 6H), 2.01 (s, 3H); LC/MS (ESI+): 308.02 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08552186B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-3624346274024ab6947dd84aba3fe65a
출처 메모uspto-grants-2013_10