戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 374792作成日:2026年10月26日

Triethylamine → N-[2-[4-(2-Pyrimidinyl)-1-piperazinyl]ethyl]tricyclo[3,3,1,13,7]decane-1-carboxamide Dihydrochloride Hydrate

https://huagongshe.com/reaction/374792

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1-Adamantanecarbonyl chlorideHCID 98915—
反応物1-Piperazineethanamine, 4-(2-pyrimidinyl)-HCID 13885358—
溶媒DichloromethaneHCID 6344—
生成物N-[2-[4-(2-Pyrimidinyl)-1-piperazinyl]ethyl]tricyclo[3,3,1,13,7]decane-1-carboxamide Dihydrochloride HydrateHCID 131717305—

反応手順

To a stirred solution of [4-(2-pyrimidinyl)piperazinyl]ethylamine (2.0 g, 0.01 mol) in 50 mL of methylene chloride, adamantane-1-carboxylic acid chloride (3.6 g, 0.018 mol) and triethylamine (2.9 g, 0.015 mol) were added. Stirring was continued at room temperature overnight. The methylene chloride solution was washed with water, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The remaining residue was dissolved in ethyl acetate (10 mL) and subjected to column chromatography using silica gel and ethyl acetate as the eluent. The title compound was separated and converted to the dihydrochloride hydrate salt with ethanolic HCl (2.4 g), m.p. 237°-239° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05482940
出典データセットuspto-grants-1996_01
ORD IDord-3fec62f3ef044aae83c18720bab50262
出典メモuspto-grants-1996_01