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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 341801생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/341801

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium borohydrideHCID 4311764—
반응물benzyl N-[4-(2-azidoethyl)piperidine-1-carboximidoyl]carbamateHCID 140379074—
촉매PalladiumHCID 23938—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물benzyl N-[4-(2-aminoethyl)piperidine-1-carboximidoyl]carbamateHCID 140379088—

반응 단계

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 tile 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05856307
출처 데이터셋uspto-grants-1999_01
ORD IDord-2ee4311c5a2e42ca94cacbcd69c4f10c
출처 메모uspto-grants-1999_01