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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12448생성일: 2026년 10월 23일

1-Isopropylpiperazine → (2-chloro-3-methyl-3H-imidazol-4-yl)-(4-isopropyl-piperazin-1-yl)-methanone

https://huagongshe.com/ko/reaction/12448

반응식

참여 물질

역할이름HCID투입량
반응물1-IsopropylpiperazineHCID 78013—
반응물1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chlorideHCID 10986715—
반응물2-Chloro-1-methyl-1H-imidazole-5-carboxylic acidHCID 53424429—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
용매DiisopropylethylamineHCID 81531—
생성물(2-chloro-3-methyl-3H-imidazol-4-yl)-(4-isopropyl-piperazin-1-yl)-methanoneHCID 59338485—

반응 단계

Under nitrogen, 2-chloro-3-methyl-3H-imidazole-4-carboxylic acid (0.161 g, 1.0 mmol) is dissolved in toluene (5 mL, anhydrous) and DIEA (0.26 mL). N-isopropylpiperazine (0.2 M in toluene; 5.5 mL; 1.1 mmol) is added followed by the slow addition of 2-chloro-1,3-dimethylimidazolinium chloride (0.3 M in acetonitrile; 4.0 mL; 1.2 mmol). The reaction mixture is stirred at rt for 2 hr and is then diluted with EtOAc and washed with NaOH (1 N). The aqueous layer is drained and reextracted with EtOAc and the combined organic extracts are extracted twice with HCl (1 N). The combined acidic aqueous extracts are washed with EtOAc then basified with NaOH (2.5 M). The resulting basic aqueous solution is extracted three times with EtOAc and the combined organic extracts are washed with brine, then dried over Na2SO4, filtered and concentrated in vacuo.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728009B1
출처 데이터셋uspto-grants-2010_06
ORD IDord-1c2f61fb48db41e3902576a0f542c4cc
출처 메모uspto-grants-2010_06