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HRID 45623作成日:2026年10月26日

Dimethylamine → methyl N-[1-(benzofuran-5-yl)-2-(dimethylamino)-2-oxoethyl]-L-leucinate

https://huagongshe.com/reaction/45623

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylamineHCID 674—
反応物TetrafluoroborateHCID 26255—
反応物1,1'-ThiocarbonyldiimidazoleHCID 80264—
反応物1H-BenzotriazoliumHCID 5210778—
反応物methyl N-{(1R)-1-(benzofuran-5-yl)-2-[(2-hydroxyphenyl)amino]-2-oxoethyl}-L-leucinateHCID 45076859—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物methyl N-[1-(benzofuran-5-yl)-2-(dimethylamino)-2-oxoethyl]-L-leucinateHCID 6884332940.5%

反応手順

A solution of methyl N-{(1R)-1-(benzofuran-5-yl)-2-[(2-hydroxyphenyl)amino]-2-oxoethyl}-L-leucinate (410 mg) and 1,1′-thiocarbonyldiimidazole (196 mg) in dichloromethane (5 ml) was left to stand for 18 hours. Water (20 l) 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, 710 mg) and a solution of dimethylamine in tetrahydrofuran (3 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 (3:1 to 1:2 cyclohexane:ethyl acetate). The required fractions were combined and evaporated to furnish methyl N-[1-(benzofuran-5-yl)-2-(dimethylamino)-2-oxoethyl]-L-leucinate (140 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541579B2
出典データセットuspto-grants-2013_09
ORD IDord-3a8f14a95948498ca5cf913034bba66f
出典メモuspto-grants-2013_09