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HRID 1254523作成日:2026年10月27日

Methanol → (S)-2-amino-N1-((S)-1,1-diethoxypropan-2-yl)-N1-(naphthalen-1-ylmethyl)-N4-tritylsuccinamide

https://huagongshe.com/reaction/1254523

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物PiperidineHCID 8082—
反応物Ethyl AcetateHCID 8857—
反応物(9H-Fluoren-9-yl)methyl (S)-1-(((S)-1,1-diethoxypropan-2-yl)(naphthalen-1-ylmethyl)amino)-1,4-dioxo-4-(tritylamino)butan-2-ylcarbamateHCID 86698534—
溶媒DichloromethaneHCID 6344—
生成物(S)-2-amino-N1-((S)-1,1-diethoxypropan-2-yl)-N1-(naphthalen-1-ylmethyl)-N4-tritylsuccinamideHCID 6707548778.2%

反応手順

(9H-Fluoren-9-yl)methyl (S)-1-(((S)-1,1-diethoxypropan-2-yl)(naphthalen-1-ylmethyl)amino)-1,4-dioxo-4-(tritylamino)butan-2-ylcarbamate (Compound III-19) 23.4 g (27 mmol) and piperidine 22.7 g (270 mmol) were added in DCM (90 ml). The mixture was stirred for 1.5 h at room temperature. The mixture was diluted with DCM (200 ml) and washed with water (150 ml×3). The solution was concentrated in vacuo. The residue was purified by column chromatography on silica gel with PE:EA=50:1 to DCM:MeOH=10:1 to give the title compound 13.6 g, (yield 78%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08455488B2
出典データセットuspto-grants-2013_06
ORD IDord-27505ddad7b74fe693078b06a63af1af
出典メモuspto-grants-2013_06