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HRID 1072633作成日:2026年10月27日

Acetic acid 2-[1-{2-[2-acetylamino-3-(hydroxyphenyl)propionyl-amino]-3-(4-fluorophenyl)propionyl}-4-(1-methylcarbamoyl-2-naphthalen-2-ylethyl)-piperazin-2-yl]ethyl ester → 2-[4-[2-[2-Acetylamino-3-(4-hydroxyphenyl)propionylamino]-3-(4-fluorophenyl)propionyl]-3-(2-hydroxyethyl)piperazin-1-yl]-n-methyl-3-naphthalene-2-yl-propionamide

https://huagongshe.com/reaction/1072633

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic acid 2-[1-{2-[2-acetylamino-3-(hydroxyphenyl)propionyl-amino]-3-(4-fluorophenyl)propionyl}-4-(1-methylcarbamoyl-2-naphthalen-2-ylethyl)-piperazin-2-yl]ethyl esterHCID 69629098—
反応物HCID 178418582HCID 178418582—
溶媒MethanolHCID 887—
生成物2-[4-[2-[2-Acetylamino-3-(4-hydroxyphenyl)propionylamino]-3-(4-fluorophenyl)propionyl]-3-(2-hydroxyethyl)piperazin-1-yl]-n-methyl-3-naphthalene-2-yl-propionamideHCID 22015683—

反応手順

To a solution acetic acid 2-[1-{2-[2-acetylamino-3-(hydroxyphenyl)-propionylamino]-3-(4-fluorophenyl)propionyl}-4-(1-methylcarbamoyl-2-naphthalen-2-ylethyl)-piperazin-2-yl]ethyl ester, 65, (7.5 g, 10 mmol) in methanol (50 mL) is added freshly prepared NaOCH3 (0.55 g, 10.1 mmol) and the solution stirred overnight. The solution is concentrated in vacuo, the resulting residue partitioned between dichloromethane and water, the organic layer is dried and concentrated in vacuo to afford the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06911447B2
出典データセットuspto-grants-2005_06
ORD IDord-bbb9ed36f3664cf4ace2b4c4adbacd65
出典メモuspto-grants-2005_06