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HRID 861作成日:2026年10月23日

Hydrochloric Acid → benzyl N-[4-(2-aminoethyl)piperidine-1-carboximidoyl]carbamate

https://huagongshe.com/ja/reaction/861

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium borohydrideHCID 4311764—
反応物benzyl N-[4-(2-azidoethyl)piperidine-1-carboximidoyl]carbamateHCID 140379074—
触媒PalladiumHCID 23938—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物benzyl N-[4-(2-aminoethyl)piperidine-1-carboximidoyl]carbamateHCID 140379088—

反応手順

To 30 ml of water was added 0.40 g of 10% Pd/C. Sodium borohydride, 1.0 g (0.031 mol), was dissolved in 30 ml of water and was added carefully to the stirred and ice-cooled slurry of Pd/C and water. 4-Azidoethyl-1-benzyloxycarbonylamidino piperidine, 2.9 g (8.8 mmol), was dissolved in 80 ml of tetrahydrofurane and this solution was added dropwise to the ice-cooled aqueous slurry above. After 4 h of stirring at room temperature the mixture was ice-cooled again and 30 ml of 2M HCl was added. The mixture was filtered through celite and the celite was rinsed with additional water. The tetrahydrofuran was evaporated and the aqueous phase was washed with ethyl acetate. The aqueous phase was made alkaline with 2M NaOH and extracted with methylene chloride three times. The combined organic phase was washed with water, dried (Na2SO4) and evaporated. The product was used in the following step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723444
出典データセットuspto-grants-1998_03
ORD IDord-2080a877db5f4bf4b20e375ca34bad46
出典メモuspto-grants-1998_03