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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2108698생성일: 2026년 10월 24일

Dimethylamine → methyl N-[1-(2,4-difluorophenyl)-2-(dimethylamino)-2-oxoethyl]-L-leucinate

https://huagongshe.com/ko/reaction/2108698

반응식

참여 물질

역할이름HCID투입량
반응물DimethylamineHCID 674—
반응물1,1'-ThiocarbonyldiimidazoleHCID 80264—
반응물1H-BenzotriazoliumHCID 5210778—
반응물methyl N-{(1R)-1-(2,4-difluorophenyl)-2-[(2-hydroxyphenyl)amino]-2-oxoethyl}-L-leucinateHCID 45076861—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물methyl N-[1-(2,4-difluorophenyl)-2-(dimethylamino)-2-oxoethyl]-L-leucinateHCID 6884265758.5%

반응 단계

A solution of methyl N-{(1R)-1-(2,4-difluorophenyl)-2-[(2-hydroxyphenyl)amino]-2-oxoethyl}-L-leucinate (203 mg) and 1,1′-thiocarbonyldiimidazole (100 mg) in dichloromethane (5 ml) was left to stand for 18 hours. Water (10□1) was added to the reaction mixture and this was then stirred rapidly for 30 minutes. After this, 1H-Benzotriazolium, 1-[bis(dimethylamino)methylene]-, tetrafluoroborate(1-), 3-oxide (TBTU, 321 mg) and a solution of dimethylamine in tetrahydrofuran (0.5 ml of 2M solution) were added. The reaction mixture was stirred for a further 18 hours and was then passed down an SPE (5 g, silica) eluting with a gradient (8:1 to 1:2 cyclohexane:ethyl acetate). The required fractions were combined and evaporated to furnish methyl N-[1-(2,4-difluorophenyl)-2-(dimethylamino)-2-oxoethyl]-L-leucinate (100 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07514437B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-9f2edd964b2d4dfdb412e519bef55eb7
출처 메모uspto-grants-2009_04