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HRID 373504作成日:2026年10月27日

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

https://huagongshe.com/reaction/373504

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4-(2-Aminoethyl)-1-cinnamylpiperazineHCID 54185928—
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-Cinnamylpiperazin-1-yl)ethyl]-6-fluoro-2',5'-dioxospiro[chroman-4,4'-imidazolidine]-2-carboxamideHCID 5714731492.9%

反応条件

温度25 °C

反応手順

To a chilled mixture (less than -5° C.) of 4-(2-aminoethyl)-1-cinnamylpiperazine (10.0 g, 40.8 mmol), 1,8-diazabicyclo[5,4,0]-7-undecene (6.20 g, 40.8 mmol) and N,N-dimethylformamide (55.0 ml, 710 mmol) was added over 30 minutes a solution of (2S,4S)-6-fluoro-2',5'-dioxospiro[chroman-4,4'-imidazolidine]-2-carbonyl chloride (Reference Example 1, 11.1 g, 37.1 mmol) in N,N-dimethylformamide (100.1 ml, 1.29 mol). After stirring the mixture for 15 hours at 25° C., the solvent was evaporated. The residue was chromatographed on silica gel, eluted with a mixture of AcOEtAcOEt/MeOH (9:1), and evaporated in vacuo to dryness to give a colorless oil of the desired compound (17.5 g, 92.6%).

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-ac134bcc6a2e48e185503fa2a5bf72a0
出典メモuspto-grants-1992_11