戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 7082作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/7082

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物beta-MethylstyreneHCID 12500—
反応物Tri-o-tolylphosphineHCID 80271—
反応物4-[2-(tert-butoxycarbonylamino)ethoxy]-N-(3-iodophenyl)-3-methoxyphenylacetamideHCID 22019609—
触媒Tetrabutylammonium ChlorideHCID 70681—
触媒palladium(II) acetateHCID 167845—
溶媒DimethylformamideHCID 6228—
生成物4-[2-(tert-Butoxycarbonylamino)ethoxy]-3-methoxy-N-[3-[(E)-2-(3-methylphenyl)vinyl]phenyl]phenylacetamideHCID 22019583152.4%

反応条件

温度97 °C

反応手順

Intermediate 4 (1 g) is dissolved in dimethylformamide (10 ml), and thereto are added 3-methylvinylbenzene (826 mg), palladium (II) acetate (105 mg), tris(2-methylphenyl)phosphine (143 mg), tetra-n-butyl ammonium chloride (130 mg), and the mixture is heated with stirring at 97° C. for 18 hours under argon atmosphere. To the reaction solution is added ethyl acetate, and the mixture is washed with water and 2 M hydrochloric acid. The organic layer is dried over sodium sulfate, and the solvent is evaporated under reduced pressure. The residue is purified by silica gel column chromatography (eluent: gradient from 0% to 100% hexane/ethyl acetate) to give 4-[2-(tert-butoxycarbonylamino)-ethoxy]-3-methoxy-N-[3-[(E)-2-(3-methylphenyl)vinyl]phenyl]phenylacetamide (370 mg). This product is treated with 10% hydrogen chloride-methanol to give the desired compound (120 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-75cc4b5bd19f4a4696cb5248dd41f0c1
出典メモuspto-grants-2006_08