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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 410372생성일: 2026년 10월 26일

2-[(4-Fluorophenoxy)methyl]oxirane → 1-[3-(3-Bromo-benzyl)-2-imino-2,3-dihydro-benzoimidazol-1-yl]-3-(4-fluoro-phenoxy)-propan-2-ol

https://huagongshe.com/reaction/410372

반응식

참여 물질

역할이름HCID투입량
반응물2-[(4-Fluorophenoxy)methyl]oxiraneHCID 2724792—
반응물1-(3-Bromo-benzyl)-1,3-dihydro-benzoimidazol-2-ylideneamineHCID 178509076—
용매EthanolHCID 702—
생성물1-[3-(3-Bromo-benzyl)-2-imino-2,3-dihydro-benzoimidazol-1-yl]-3-(4-fluoro-phenoxy)-propan-2-olHCID 4624121246.2%

반응 단계

To a solution of 1-(3-bromo-benzyl)-1,3-dihydro-benzoimidazol-2-ylideneamine (0.50 g, 1.66 mmol) in EtOH (30 ml) at rt was added 2-(4-fluoro-phenoxymethyl)-oxirane (278 mg, 1.66 mmol). The reaction was heated to reflux where it was maintained for 24 h. After this time, additional 2-(4-fluoro-phenoxymethyl)-oxirane (278 mg, 1.66 mmol) was introduced and the reaction was heated to reflux where it was left for a further 6 h. The mixture was cooled to rt and concentrated under reduced pressure. Purification by column chromatography on silica eluting with MeOH/dichloromethane (2-5% gradient) provided 1-[3-(3-bromo-benzyl)-2-imino-2,3-dihydro-benzoimidazol-1-yl]-3-(4-fluoro-phenoxy)-propan-2-ol (361 mg, 46%). HPLC-MS 470, 472 [M+1]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759520B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-b7767a325a864da28b7ffab11bec11cf
출처 메모uspto-grants-2014_06