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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80208생성일: 2026년 10월 24일

Methanol → 1-[4-(Cyclopropyl-hydroxy-methyl)-3-fluoro-phenyl)-3-(4-methyl-pyridin-3-yl)-imidazolidin-2-one

https://huagongshe.com/ko/reaction/80208

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물2-Fluoro-4-[3-(4-methyl-pyridin-3-yl)-2-oxo-imidazolidin-1-yl]-benzaldehydeHCID 59636164—
반응물HCID 178418630HCID 178418630—
용매ChloroformHCID 6212—
용매TetrahydrofuranHCID 8028—
생성물1-[4-(Cyclopropyl-hydroxy-methyl)-3-fluoro-phenyl)-3-(4-methyl-pyridin-3-yl)-imidazolidin-2-oneHCID 5963614199.41%

반응 단계

A 0.5M solution of cyclopropyl magnesium bromide in THF (2.4 mL, 1.170 mmol) was added dropwise to 2-fluoro-4-[3-(4-methyl-pyridin-3-yl)-2-oxo-imidazolidin-1-yl]-benzaldehyde (I-121a: 175 mg, 0.585 mmol) in dry THF (10 mL) at 0° C. under nitrogen atmosphere. The resulting mixture was stirred at room temperature for 3 hours. The reaction was monitored by TLC (5% MeOH in CHCl3). The reaction mixture was quenched with aqueous NH4Cl solution and the THF layer was concentrated. The aqueous layer was extracted with ethylacetate. The organic layer was dried over Na2SO4 and concentrated to afford the crude product. Purification by column chromatography on silica gel (3% MeOH in CHCl3), followed by hexane wash, afforded 200 mg of the product (99.41% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE045173E1
출처 데이터셋uspto-grants-2014_09
ORD IDord-c323f36ffc3a460b8657f46c3124e82d
출처 메모uspto-grants-2014_09