Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1160119생성일: 2026년 10월 25일
4-Methyl-3-nitroaniline → N-(4-Methyl-3-nitro-phenyl)-4-(4-methyl-piperazin-1-ylmethyl)-benzamide
https://huagongshe.com/reaction/1160119
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Methyl-3-nitroaniline | HCID 8390 | — |
| 반응물 | Methyl 4-((4-methylpiperazin-1-yl)methyl)benzoate | HCID 782222 | — |
| 반응물 | Potassium sodium tartarate | HCID 9855836 | — |
| 반응물 | Trimethylaluminum | HCID 16682925 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | tert-Butyl methyl ether | HCID 15413 | — |
| 생성물 | N-(4-Methyl-3-nitro-phenyl)-4-(4-methyl-piperazin-1-ylmethyl)-benzamide | HCID 29984087 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07816359B2 |
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| 출처 데이터셋 | uspto-grants-2010_10 |
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| ORD ID | ord-acf7ac18a4634b81b708445c06452043 |
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| 출처 메모 | uspto-grants-2010_10 |
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