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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2222015생성일: 2026년 10월 25일

Sodium hydride → 3-([4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl](methyl)amino)-1-phenyl-1H-pyrazole-4-carbaldehyde

https://huagongshe.com/reaction/2222015

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물4-(4-Chloromethyl-2-methoxyphenoxymethyl)-2-(2-furyl)-5-methyloxazoleHCID 22344597—
반응물3-(methylamino)-1-phenyl-1H-pyrazole-4-carbaldehydeHCID 23076364—
용매DimethylformamideHCID 6228—
생성물3-([4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl](methyl)amino)-1-phenyl-1H-pyrazole-4-carbaldehydeHCID 8660592550.3%

반응 단계

To a solution of 3-(methylamino)-1-phenyl-1H-pyrazole-4-carbaldehyde (150 mg) in N,N-dimethylformamide (5 mL) was added sodium hydride (60% in oil, 36 mg) on an ice bath, and the mixture was stirred for 30 min. To the reaction mixture was added 4-[(4-chloromethyl-2-methoxyphenoxy)methyl]-2-(2-furyl)-5-methyl-1,3-oxazole (227 mg), and the mixture was further stirred at room temperature for 1 hr. Ice water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to flash silica gel column chromatography and eluted with ethyl acetate-hexane (1:9 to 6:4, v/v) to give 3-([4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl](methyl)amino)-1-phenyl-1H-pyrazole-4-carbaldehyde as colorless crystals (170.4 mg, yield 46%). melting point: 101-102° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07368578B2
출처 데이터셋uspto-grants-2008_05
ORD IDord-cc1af7221db54bea9531fe10f60e1f05
출처 메모uspto-grants-2008_05