戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1684698作成日:2026年10月25日

Water → (S)-N-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl]-1,4-dihydro-pyridine

https://huagongshe.com/reaction/1684698

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物GlutaraldehydeHCID 3485—
反応物p-Toluenesulfonic acidHCID 6101—
反応物Tetrahydrofurane dichloromethaneHCID 21919333—
反応物phthalimido-(S)-phenyalanine amideHCID 53840537—
溶媒DichloromethaneHCID 6344—
生成物(S)-N-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl]-1,4-dihydro-pyridineHCID 15380836—

反応手順

Combine phthalimido-(S)-phenyalanine amide (3.0 g, 10 mmol) and a solution of glutaric dialdehyde (2.0 g, 50% by weight in water) in dichloromethane (200 mL). Heat to reflux with azeotropic removal of water from the refluxate. Add p-toluenesulfonic acid (60 mg). Continue heating at reflux. Pass the refluxate through oven dried 4Å molecular sieves. After 4 days, cool the reaction mixture to ambient temperature. Extract with 5% sodium bicarbonate solution. Extract the 5% sodium bicarbonate solution with dichloromethane. Combine the organic layers and dry over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 5% tetrahydrofuran/dichloromethane to give the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05641880
出典データセットuspto-grants-1997_06
ORD IDord-179faffd5a1a40bab5199a8c4f62a804
出典メモuspto-grants-1997_06