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HRID 373507作成日:2026年10月27日

Dimethylformamide → (2S,4S)-N-[2-(4-Benzylpiperidin-1-yl)ethyl]-6-fluoro-2'5'-dioxospiro[chroman-4,4'-imidazolidine]-2-carboxamide

https://huagongshe.com/reaction/373507

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物2-(4-Benzylpiperidin-1-yl)ethan-1-amineHCID 2779831—
反応物(2S,4S)-6-fluoro-2',5'-dioxospiro[chroman-4,4'-imidazolidine]-2-carbonyl chlorideHCID 57210646—
生成物(2S,4S)-N-[2-(4-Benzylpiperidin-1-yl)ethyl]-6-fluoro-2'5'-dioxospiro[chroman-4,4'-imidazolidine]-2-carboxamideHCID 1864889450%

反応条件

温度-30 °C

反応手順

A mixture of N-(2-aminoethyl)-4-benzylpiperidine (13.0 g, 59.6 mmol), 1,8-diazabicyclo[5,4,0]-7-undecene (10.9 g, 71.7 mmol) and N,N-dimethylformamide (90.0 ml, 1.16 mol) was chilled to -30° C. To the mixture was added over 30 minutes a solution of (2S, 4S)-6-fluoro-2',5'-dioxospiro[chroman-4,4'-imidazolidine]-2-carbonyl chloride (Reference Example, 18.0 g, 60.3 mmol) in N,N-dimethylformamide (90.0 ml, 1.16 mol) and the mixture was stirred for 15 hours at temperature of 15°-25° C. After distilling off the solvent, the reaction mixture was chromatographed on silica gel, eluted with CH2Cl2 /MeOH (9/1) and evaporated in vacuo to dryness to give the desired compound (14.3 g, 50.0%) as colorless amorphous substance.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05164391
出典データセットuspto-grants-1992_11
ORD IDord-c6d5e1d3fcb54a83a48220d146ac0044
出典メモuspto-grants-1992_11