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HRID 978199作成日:2026年10月25日

Acetic Anhydride → Rolziracetam

https://huagongshe.com/reaction/978199

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物DiketeneHCID 12661—
反応物2,2,6-Trimethyl-4H-1,3-dioxin-4-oneHCID 79368—
反応物3-(5-Oxopyrrolidin-2-yl)propanoic acidHCID 4585667—
生成物RolziracetamHCID 71893—

反応手順

In a process for preparing dihydro-1H-pyrrolizine-3,5(2H, 6H)-dione comprising the steps of catalytically hydrogenating an ester of 4-(hydroxyimino)heptanedioic acid and subsequently cyclizing the resulting product to dihydro-1H-pyrrolizine-3,5(2H,6H)-dione, the improvement comprises reacting an alcoholic solution of a mono(lower alkyl) ester of 4-(hydroxyimino)heptanedioic acid, wherein lower alkyl comprises from one to three carbon atoms, with hydrogen gas at a temperature of about 60° C. in the presence of rhodium/alumina catalyst and a tertiary lower alkyl amine, wherein said lower alkyl amine comprises from three to nine carbon atoms, to produce 5-oxo-2-pyrrolidinepropanoic acid; and thereafter heating said 5-oxo-2-pyrrolidinepropanoic acid in the presence of a cyclizing agent selected from acetic anhydride, 2,2,6-trimethyl-1,3-dioxen-4-one, and diketene at a temperature of about 90° C. to produce dihydro-1H-pyrrolizine-3,5(2H,6H)-dione.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04663464
出典データセットuspto-grants-1987_05
ORD IDord-a0894d6580a741cba8f872bfbd9b211b
出典メモuspto-grants-1987_05