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HRID 2361986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)(naphthalen-1-ylmethyl)amino)-1-oxopropan-2-ylcarbamate

https://huagongshe.com/reaction/2361986

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-(naphthalen-1-ylmethyl)propan-2-amineHCID 67075196—
生成物(9H-fluoren-9-yl)methyl (S)-3-(4-tert-butoxyphenyl)-1-(((S)-1,1-diethoxypropan-2-yl)(naphthalen-1-ylmethyl)amino)-1-oxopropan-2-ylcarbamateHCID 8669852679.1%

反応手順

According to the procedure described in the synthesis method of Compound III-5, (S)-1,1-diethoxy-N-(naphthalen-1-ylmethyl)propan-2-amine (Compound IX-6) (686 mg, 2.4 mmol) was coupled with (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(4-tert-butoxyphenyl)propanoic acid (1.15 g, 2.51 mmol) and the obtained residue was purified by Büch silica gel column chromatography (eluent: n-hexane:ethyl acetate=7:3) to obtain the title compound (1.384 g, 79%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08691819B2
出典データセットuspto-grants-2014_04
ORD IDord-d0083259c19e4c049c2e897761335378
出典メモuspto-grants-2014_04