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HRID 273291생성일: 2026년 10월 25일

4-Methyl-3-nitroaniline → N-(4-Methyl-3-nitro-phenyl)-4-(4-methyl-piperazin-1-ylmethyl)-benzamide

https://huagongshe.com/reaction/273291

반응식

참여 물질

역할이름HCID투입량
반응물4-Methyl-3-nitroanilineHCID 8390—
반응물Methyl 4-((4-methylpiperazin-1-yl)methyl)benzoateHCID 782222—
반응물Potassium sodium tartarateHCID 9855836—
반응물TrimethylaluminumHCID 16682925—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
용매tert-Butyl methyl etherHCID 15413—
생성물N-(4-Methyl-3-nitro-phenyl)-4-(4-methyl-piperazin-1-ylmethyl)-benzamideHCID 29984087—

반응 조건

온도0 °C

반응 단계

A solution of trimethylaluminium (2M in toluene, 1.3 ml, 2.6 mmol) is added over a period of 5 min to a solution of 3-nitro-4-methyl-aniline(152 mg, 1.00 mmol) and 4-(4-methyl-piperazin-1-ylmethyl)-benzoic acid methyl ester (248 mg, 1.00 mmol) in toluene (3.0 ml) at 45° C. under an atmosphere of argon. After gas evolution ceases, the dark brown reaction mixture is stirred 30 min before being cooled to 0° C. An aqueous saturated solution of potassium-sodium tartrate (20 ml), t-butyl methyl ether (15 ml) and methylene chloride (10 ml) are added sequentially. The organic phase is separated and washed with aqueous saturated NaHCO3 (10 ml) and aqueous saturated NaCl (10 ml). The aqueous phases are back-extracted with t-butyl methyl ether (2×15 ml). The organic phases are combined, dried over MgSO4 and concentrated in vacuo to give 383 mg (96 area % by HPLC) of the title compound as pale yellow crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456283B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-e01e68b5d0e6410ebe169c13eb7d4d6c
출처 메모uspto-grants-2008_11