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HRID 215952作成日:2026年10月26日

Triethylamine → HCID 178525098、化合物

https://huagongshe.com/reaction/215952

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物1-Benzyl 4-methyl 4-(2-oxoethyl)piperidine-1,4-dicarboxylateHCID 58893182—
反応物HCID 178479277HCID 178479277—
溶媒1,2-DichloroethaneHCID 11—
溶媒DichloromethaneHCID 6344—
生成物HCID 178525098HCID 17852509872.4%

反応手順

A mixture of 1-benzyl 4-methyl 4-(2-oxoethyl)piperidine-1,4-dicarboxylate (4.80 g, 0.0150 mol), cis-4-aminocyclohexanol hydrochloride (2.5 g, 0.016 mol) and triethylamine (3.3 mL, 0.024 mol) in 1,2-dichloroethane (30.0 mL) was stirred at room temperature for 30 min. To the mixture was added sodium triacetoxyborohydride (7.9 g, 0.038 mol) with stirring. The mixture was stirred at room temperature for 1 h, then was heated at 80° C. for 2 h. After cooling, the mixture was diluted with dichloromethane, and washed with IN HCl solution, NaHCO3 (7.5%), water, and brine successively, dried over Na2SO4, filtered, and concentrated. The residue was purified by flash chromatography to give benzyl 2-(cis-4-hydroxycyclohexyl)-1-oxo-2,8-diazaspiro[4.5]decane-8-carboxylate (4.20 g, 72.0%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193207B2
出典データセットuspto-grants-2012_06
ORD IDord-af0a5c1b5a764d38b93dc828e33884af
出典メモuspto-grants-2012_06