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HRID 11558생성일: 2026년 10월 23일

Hydrazine hydrate (1:1) → N~1~-[3-(4-Methylpiperazin-1-yl)propyl]benzene-1,4-diamine

https://huagongshe.com/ko/reaction/11558

반응식

참여 물질

역할이름HCID투입량
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물N-[3-(4-methylpiperazin-1-yl)propyl]-4-nitro-1-aminobenzeneHCID 21975010—
촉매NickelHCID 935—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물N~1~-[3-(4-Methylpiperazin-1-yl)propyl]benzene-1,4-diamineHCID 21975027—

반응 조건

온도50 °C

반응 단계

A suspension of 0.1385 gms. of [3-(4-methyl-piperazin-1-yl)-propyl]-(4-nitro-phenyl)-amine in 3 mL of ethanol is heated to 50° C. Once dissolution is achieved 0.144 mL hydrazine monohydrate is addded to the solution. A Raney nickel slurry in water is added to the 50° C. solution dropwise, waiting after each addition for the gas evolution to cease. Sufficient quantities of Raney nickel have been added when continued addition of Raney nickel causes no further gas evolution. The reaction is then maintained at 50° C. for an additional hour, and subsequently is cooled to room temperature. The reaction mixture is filtered through a pad of celite (rinsing the pad with methanol). N-[3-(4-Methyl-piperazin-1-yl)-propyl]-benzene-1,4-diamine (0.116 gms.) is isolated upon evaporation of the filtrate, and is subsequently used without purification in the reaction of Example 302.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098236B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-eb1ff254344f4230a9d813e4b5254294
출처 메모uspto-grants-2006_08