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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58168생성일: 2026년 10월 26일

1-Ethylpiperazine → 4-(4-Ethyl-piperazin-1-ylmethyl)-2-nitro-phenylamine

https://huagongshe.com/reaction/58168

반응식

참여 물질

역할이름HCID투입량
반응물1-EthylpiperazineHCID 79196—
반응물Sodium borohydrideHCID 4311764—
반응물4-Amino-3-nitrobenzaldehydeHCID 13237703—
촉매HCID 178460666HCID 178460666—
용매MethanolHCID 887—
용매Ethyl AcetateHCID 8857—
생성물4-(4-Ethyl-piperazin-1-ylmethyl)-2-nitro-phenylamineHCID 5504639534%

반응 단계

To a stirred solution of 1-ethyl-piperazine (1.37 g, 12 mmol) in MeOH (30 mL) was added Ti(OiPr)4 (1.73 g, 6 mmol). Then the solution was stirred at room temperature for 15 min. Then 4-amino-3-nitro-benzaldehyde (Procedure 2F, steps a-b, 1.5 g, 9 mmol) in MeOH (10 mL) was added and the solution was stirred at room temperature overnight. Then NaBH4 (380 mg, 10 mmol) was added and the solution was stirred at room temperature for 1 hour. The solution was diluted with EtOAc and filtered. The filtrate was washed with water and brine, dried over anhydrous Na2SO4. Concentration gave product, which was purified by flash chromatography on silica to obtain the title compound (800 mg, yield: 34%). MS (ESI): 265 [M+H]+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434697B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-09b9e11eaef04abeafbfb647896bb2e2
출처 메모uspto-grants-2016_09