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HRID 8536作成日:2026年10月24日

Cyclohexene → HCID 178418962、化合物

https://huagongshe.com/ja/reaction/8536

反応式

関与物質

役割名称HCID仕込み量
反応物CyclohexeneHCID 8079—
反応物2-acetylamino-N-[2-[2-(1-benzyl-1H-imidazol-4-ylmethyl)-5-naphthalen-2-ylmethyl-3-oxo-piperazin-1-yl]-1-(4-fluorobenzyl)-2-oxo-ethyl]-3-(4-hydroxyphenyl)-propionamideHCID 69652750—
触媒PalladiumHCID 23938—
溶媒Acetic acid ethanolHCID 18476134—
生成物HCID 178418962HCID 178418962—

反応手順

2-acetylamino-N-[2-[2-(1-benzyl-1H-imidazol-4-ylmethyl)-5-naphthalen-2-ylmethyl-3-oxo-piperazin-1-yl]-1-(4-fluorobenzyl)-2-oxo-ethyl]-3-(4-hydroxyphenyl)propionamide, 73, (0.22 g, 0.28 mmol) is dissolved in ethanol/acetic acid (4:1) (3 mL). Cyclohexene (3 mL) and Pd-black are added and the solution is refluxed with periodic replenishment of cyclohexene. The reaction is monitored by TLC and after 2 days is cooled and filtered through Celite to remove the catalyst. The filtrate is concentrated in vacuo to afford an oil which is purified by reverse phase C18 prep HPLC to afford the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087759B2
出典データセットuspto-grants-2006_08
ORD IDord-c890d2c1d61a43e1a16a98e903c1d8ab
出典メモuspto-grants-2006_08