戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 51639作成日:2026年10月23日

Dichloromethane → [4-(5-(Cyclopropyl-amino)-8,8-dimethyl-5,6,7,8-tetrahydro-naphthalene-2-yl-ethynyl)-2-fluoro-phenyl] acetic acid ethyl ester

https://huagongshe.com/ja/reaction/51639

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物CyclopropylamineHCID 69828—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物[2-Fluoro-4-(8,8-dimethyl-5-oxo-5,6,7,8-tetrahydronaphthalene-2-ylethynyl)phenyl]acetic acid ethyl esterHCID 69548870—
溶媒Acetic AcidHCID 176—
溶媒AcetonitrileHCID 6342—
溶媒HexaneHCID 8058—
溶媒Ethyl AcetateHCID 8857—
生成物[4-(5-(Cyclopropyl-amino)-8,8-dimethyl-5,6,7,8-tetrahydro-naphthalene-2-yl-ethynyl)-2-fluoro-phenyl] acetic acid ethyl esterHCID 69548141—

反応手順

Following general procedure G and using [2-fluoro-4-(8,8-dimethyl-5-oxo-5,6,7,8-tetrahydro-naphthalene-2-ylethynyl) phenyl]acetic acid ethyl ester (Compound 14, 0.258 g, 0.68 mmol), dichloromethane (4 mL), acetonitrile(2 mL), cyclopropyl amine(1 mL, 14.45 mmol), acetic acid (1 mL) and sodium cyanoborohydride (0.266 g, 4.23 mmol) followed by flash column chromatography over silica gel (230-400 mesh) using 16-20-25% ethyl acetate in hexane as the eluent, the title compound was obtained as a pale yellow oil (0.21 g, 73%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713647B2
出典データセットuspto-grants-2004_03
ORD IDord-c05d2c36124b4a678cc5fec5e58352e6
出典メモuspto-grants-2004_03