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HRID 3674作成日:2026年10月23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/ja/reaction/3674

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 4 Å 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 Na2 SO4, 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US05734049
出典データセットuspto-grants-1998_03
ORD IDord-664817258c1d475a9aa4855277b7c19b
出典メモuspto-grants-1998_03