돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 412943생성일: 2026년 10월 26일

Water → 1-Acetyl-N-{3-[4-(4-aminoanilino)-1-piperidinyl]propyl}-N-(3,4-dichlorophenyl)-4-piperidinecarboxamide

https://huagongshe.com/reaction/412943

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Ethyl AcetateHCID 8857—
반응물Sodium borohydrideHCID 4311764—
반응물1-Acetyl-N-(3,4-dichlorophenyl)-N-{3-[4-(4-nitroanilino)-1-piperidinyl]propyl}-4-piperidinecarboxamideHCID 18539069—
촉매Nickel(II) bromideHCID 278492—
용매Diisopropylether hexaneHCID 21881879—
생성물1-Acetyl-N-{3-[4-(4-aminoanilino)-1-piperidinyl]propyl}-N-(3,4-dichlorophenyl)-4-piperidinecarboxamideHCID 1853886465.4%

반응 단계

To a solution of the compound obtained in Example 219 (162 mg, 0.26 mmol) in methanol/THF (1/1, 10 mL) were added nickel bromide (II)(5.7 mg) and sodium borohydride (40 mg, 1.1 mmol), and the mixture was stirred at room temperature for 10 minutes. To the reaction mixture were added ethyl acetate (20 mL) and water (20 mL), and the insolubles were filtered off with Celite. The organic layer was washed with saturated aqueous solution of sodium chloride (10 ml), dried with anhydrous sodium sulfate and concentrated under reduced pressure. The concentrate was subjected to flash column chromatography (alumina 2 g, ethyl acetate/methanol=1/0 to 10/1), and the desired fraction was concentrated under reduced pressure to give the titled compound (99 mg, 0.17 mmol, Yield 64%) as pale yellow amorphous substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06562978B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-0cc3015dd9da46a6bd9631c66d71c1b9
출처 메모uspto-grants-2003_05