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HRID 1450705生成日期:2026年10月23日

海萝胶 → benzyl N-[4-(2-aminoethyl)piperidine-1-carboximidoyl]carbamate

https://huagongshe.com/zh-CN/reaction/1450705

反应方程式

参与物

角色名称HCID投料
反应物海萝胶HCID 313—
反应物硼氢化钠HCID 4311764—
反应物benzyl N-[4-(2-azidoethyl)piperidine-1-carboximidoyl]carbamateHCID 140379074—
催化剂钯HCID 23938—
溶剂聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 962—
溶剂四氢呋喃HCID 8028—
产物benzyl N-[4-(2-aminoethyl)piperidine-1-carboximidoyl]carbamateHCID 140379088—

反应步骤

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.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US05602253
来源数据集uspto-grants-1997_02
ORD IDord-39ad06abf1904082bc3f4647d3099b3e
来源说明uspto-grants-1997_02