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HRID 3894作成日:2026年10月24日

Ammonia → 1-(Pyrid-2-oyl)-3-[1-(naphth-2-ylmethyl)piperid-4-yl]urea

https://huagongshe.com/ja/reaction/3894

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Ethyl 2-pyridinecarboxylateHCID 17307—
反応物SodiumHCID 5360545—
反応物[1-(Naphth-2-ylmethyl)piperid-4-yl]ureaHCID 13145794—
生成物1-(Pyrid-2-oyl)-3-[1-(naphth-2-ylmethyl)piperid-4-yl]ureaHCID 1976239832.5%

反応手順

Sodium (0.1 g, 4.35 mmol) in liquid ammonia (100-150 cm3) was stirred until the blue colour was discharged. A bomb was charged with [1-(Naphth-2-yl-methyl)piperid-4-yl]urea (0.83 g, 2.93 mmol) and the liquid ammonia solution was added. The mixture was stirred at room temperature for 2 days then the bomb was cooled to -78° C., and ethyl picolinate (0.6 g, 3.97 mmol) was added. Stirring was continued for 3 hours at room temperature then the ammonia was allowed to evaporate and the gummy residue triturated with water then ethyl acetate. The ethyl acetate suspension was filtered to give recovered [1-(naphth-2-ylmethyl)piperid-4-yl]urea (0.33 g). The filtrate was evaporated and the residue chromatographed on silica eluting with chloroform then chloroform: ethyl acetate 4:1 to give the title compound (0.37 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04722930
出典データセットuspto-grants-1988_02
ORD IDord-5a710b5c50314be3848a9b1928e8c6b3
出典メモuspto-grants-1988_02