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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1348958생성일: 2026년 10월 27일

Triphenylphosphine → 5-[4-(2-methyl-quinolin-4-ylmethoxy)-phenylsulfanylmethyl]-2-oxo-2,3-dihydro-1H-imidazole-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/1348958

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diethyl azodicarboxylateHCID 5462977—
반응물(2-Methylquinolin-4-yl)methanolHCID 10149033—
반응물5-(4-hydroxy-phenylsulfanyl methyl)-2-oxo-2,3-dihydro-1H-imidazole-4-carboxylic acid methyl esterHCID 71195099—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물5-[4-(2-methyl-quinolin-4-ylmethoxy)-phenylsulfanylmethyl]-2-oxo-2,3-dihydro-1H-imidazole-4-carboxylic acid methyl esterHCID 694323298%

반응 단계

To a solution of DEAD (81 mg, 0.46 mmol) in 3 mL of THF at 0° C. was added PPh3 (120 mg, 0.46 mmol). After dissolution of PPh3, 4d (100 mg, 0.31 mmol) was added and the solution was stirred for 15 min. (2-methyl-4-quinolinyl)methanol was then added as a solid. After stirring for 2 h, 3 mL of DMF was added to aid dissolution. The mixture was stirred at room temperature overnight before it was quenched with water. The solution was extracted with CH2Cl2 and the organic layer was dried over MgSO4. After filtration and concentration, the residue was purified by flash column chromatography to provide 5-[4-(2-methyl-quinolin-4-ylmethoxy)-phenylsulfanylmethyl]-2-oxo-2,3-dihydro-1H-imidazole-4-carboxylic acid methyl ester 4e (11 mg, 8%). MS (ESI+) (M+1)=436.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07211671B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-f3ab5768211b4e6a88490fda4322a720
출처 메모uspto-grants-2007_05