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HRID 2274670作成日:2026年10月27日

Fmoc-L-Tyr(tBu)-OH → (9H-fluoren-9-yl)methyl (S)-3-(4-tert-butoxyphenyl)-1-(((S)-1,1-diethoxypropan-2-yl)(quinoxalin-5-ylmethyl)amino)-1-oxopropan-2-ylcarbamate

https://huagongshe.com/reaction/2274670

反応式

関与物質

役割名称HCID仕込み量
反応物Fmoc-L-Tyr(tBu)-OHHCID 10895791—
反応物(S)-1,1-diethoxy-N-(quinoxalin-5-ylmethyl)propan-2-amineHCID 67075656—
生成物(9H-fluoren-9-yl)methyl (S)-3-(4-tert-butoxyphenyl)-1-(((S)-1,1-diethoxypropan-2-yl)(quinoxalin-5-ylmethyl)amino)-1-oxopropan-2-ylcarbamateHCID 8669853048.3%

反応手順

According to the procedure described in the synthesis method of Compound III-5, (S)-1,1-diethoxy-N-(quinoxalin-5-ylmethyl)propan-2-amine (Compound IX-12) (1.93 g, 6.65 mmol) was coupled with (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(4-tert-butoxyphenyl)propanoic acid (3.36 g, 7.31 mmol) and the obtained residue was purified by Büch silica gel column chromatography (eluent: chloroform:methanol=100:0 to 98:2) to obtain the title compound (2.35 g, 48%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09126981B2
出典データセットuspto-grants-2015_09
ORD IDord-8b7452dcb4114811818656491c7e4905
出典メモuspto-grants-2015_09