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HRID 7083作成日:2026年10月23日

4-[2-(tert-Butoxycarbonylamino)ethoxy]-3-methoxy-N-[3-[(E)-2-(3-methylphenyl)vinyl]phenyl]phenylacetamide → 4-[2-(tert-butoxycarbonylamino)ethoxy]-3-methoxy-N-[3-[2-(3-methylphenyl)ethyl]phenyl]phenylacetamide

https://huagongshe.com/ja/reaction/7083

反応式

関与物質

役割名称HCID仕込み量
反応物4-[2-(tert-Butoxycarbonylamino)ethoxy]-3-methoxy-N-[3-[(E)-2-(3-methylphenyl)vinyl]phenyl]phenylacetamideHCID 22019583—
触媒PalladiumHCID 23938—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
生成物4-[2-(tert-butoxycarbonylamino)ethoxy]-3-methoxy-N-[3-[2-(3-methylphenyl)ethyl]phenyl]phenylacetamideHCID 2201959779.7%

反応手順

4-[2-(tert-Butoxycarbonylamino)ethoxy]-3-methoxy-N-[3-[(E)-2-(3-methylphenyl)vinyl]phenyl]phenylacetamide (100 mg) is dissolved in methanol (10 ml) and acetic acid (1 ml), and thereto is added 10% palladium on carbon (10 mg), and the mixture is subjected to catalytic hydrogenation at 50° C. The catalyst is removed by filtration, and the solvent is evaporated to give 4-[2-(tert-butoxycarbonylamino)ethoxy]-3-methoxy-N-[3-[2-(3-methylphenyl)ethyl]phenyl]phenylacetamide (80 mg). This product is treated with 10% hydrogen chloride-methanol to give the desired compound (50 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084176B2
出典データセットuspto-grants-2006_08
ORD IDord-6faf8d70cb6a4ac0804d8ed31f4ed67f
出典メモuspto-grants-2006_08