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HRID 1254512作成日:2026年10月26日

Piperidine → (S)-2-amino-3-(4-tert-butoxyphenyl)-N-((S)-1,1-diethoxypropan-2-yl)-N-(quinolin-8-ylmethyl)propanamide

https://huagongshe.com/reaction/1254512

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物(9H-fluoren-9-yl)methyl (S)-3-(4-tert-butoxyphenyl)-1-(((S)-1,1-diethoxypropan-2-yl)(quinolin-8-ylmethyl)amino)-1-oxopropan-2-ylcarbamateHCID 86698527—
生成物(S)-2-amino-3-(4-tert-butoxyphenyl)-N-((S)-1,1-diethoxypropan-2-yl)-N-(quinolin-8-ylmethyl)propanamideHCID 6707520877%

反応手順

According to the procedure described in the synthesis method of Compound IV-1, (9H-fluoren-9-yl)methyl (S)-3-(4-tert-butoxyphenyl)-1-(((S)-1,1-diethoxypropan-2-yl)(quinolin-8-ylmethyl)amino)-1-oxopropan-2-ylcarbamate (Compound III-3) 2.41 g (3.31 mmol) was treated with piperidine and purified on silica gel column chromatography (n-hexane:ethyl acetate=9:1, chloroform:methanol=100:0 and 8:2) to obtain the title compound 1.29 g (77%).

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-fbf1a03733a24ab98f6787055b9c2dbb
出典メモuspto-grants-2013_06