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HRID 241556作成日:2026年10月26日

Dimethylformamide dimethyl acetal → tert-butyl 3-[(dimethylamino)methylene]-4-oxotetrahydro-1(2H)-pyridinecarboxylate

https://huagongshe.com/reaction/241556

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethylformamide dimethyl acetalHCID 78373—
反応物tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
溶媒DimethylformamideHCID 6228—
生成物tert-butyl 3-[(dimethylamino)methylene]-4-oxotetrahydro-1(2H)-pyridinecarboxylateHCID 53395404—

反応手順

A solution of tert-butyl 4-oxo-1-piperidinecarboxylate (8.73 g, 44 mmol) and N,N-dimethylformamide dimethyl acetal (5.8 mL, 44 mmol) in 80 mL of dry N,N-dimethylformamide was warmed at 80° C. for 18 h. The solution was cooled and concentrated under reduced pressure, and the residue was partitioned between ethyl acetate and water. The mixture was filtered through a pad of Celite, and the organic layer was separated, washed with saturated brine, dried over magnesium sulfate and concentrated under reduced pressure to afford the title compound as an orange oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653059B2
出典データセットuspto-grants-2014_02
ORD IDord-f02ff545749046408d8200fa756444d7
出典メモuspto-grants-2014_02