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HRID 2274665作成日:2026年10月26日

Fmoc-L-Tyr(tBu)-OH → (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

https://huagongshe.com/reaction/2274665

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-(quinolin-8-ylmethyl)propan-2-amineHCID 67074994—
生成物(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 8669852771.8%

反応手順

According to the procedure described in the synthesis method of Compound III-5, (S)-1,1-diethoxy-N-(quinolin-8-ylmethyl)propan-2-amine (Compound IX-7) (1.33 g, 4.6 mmol) was coupled with (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(4-tert-butoxyphenyl)propanoic acid (2.22 g, 4.84 mmol) and the obtained residue was purified by Büch silica gel column chromatography (eluent: n-hexane:ethyl acetate=4:6) to obtain the title compound (2.41 g, 68%).

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-2c2e9fa3b18d4e4abd549e481ff5f2db
出典メモuspto-grants-2015_09