戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2238521作成日:2026年10月26日

Ethylmorpholine → N-{[2-chloro-3-(trifluoromethyl)phenyl]methyl}-5-oxo-1-(phenylmethyl)-D-prolinamide

https://huagongshe.com/reaction/2238521

反応式

関与物質

役割名称HCID仕込み量
反応物EthylmorpholineHCID 7525—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物Sodium BicarbonateHCID 516892—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物2-Chloro-3-(trifluoromethyl)benzylamineHCID 5224207—
反応物(S)-1-Benzyl-5-carboxy-2-pyrrolidinoneHCID 10900113—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物N-{[2-chloro-3-(trifluoromethyl)phenyl]methyl}-5-oxo-1-(phenylmethyl)-D-prolinamideHCID 67463195—

反応手順

5-oxo-1-(phenylmethyl)proline (0.100 g, 0.46 mmol, prepared as described below) was dissolved in a mixture of dichloromethane (2.5 ml) and dimethylformamide (0.5 ml) and to this were added N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.105 g, 0.55 mmol), 1-hydroxybenzotriazole (0.074 g, 0.55 mmol), and N-ethyl morpholine (0.143 ml, 1.37 mmol). The mixture was stirred for 10 minutes and then {[2-chloro-3-(trifluoromethyl)phenyl]methyl}amine (0.115 g, 0.55 mmol) was added and the mixture was stirred for 1 hr. Saturated aqueous sodium hydrogen carbonate (10 ml) was added and the mixture stirred vigorously for 15 minutes. The organic phase was separated with a phase separator and the aqueous phase was washed with further aliquots of dichloromethane (3×10 ml). The organic fractions were combined and dried over magnesium sulphate. The solvent was then evaporated and the residue was purified by mass-directed automated HPLC to give pure N-{[2-chloro-3-(trifluoromethyl)phenyl]methyl}-5-oxo-1-(phenylmethyl)-D-prolinamide

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07718693B2
出典データセットuspto-grants-2010_05
ORD IDord-09fa240a60034ec7bae28a16d665c3df
出典メモuspto-grants-2010_05