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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4226생성일: 2026년 10월 26일

1,1'-Carbonyldiimidazole → N-(1-Methylethyl)-N'-[3-(4-methyl-1-piperazinyl)propyl]-N-[2-(phenylsulfonyl)ethyl]urea maleate

https://huagongshe.com/reaction/4226

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물1-(3-Aminopropyl)-4-methylpiperazineHCID 78328—
반응물Maleic AcidHCID 444266—
반응물N-(2-phenylsulfonylethyl)-2-propanamineHCID 13655034—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물N-(1-Methylethyl)-N'-[3-(4-methyl-1-piperazinyl)propyl]-N-[2-(phenylsulfonyl)ethyl]urea maleateHCID 1405029068.8%

반응 단계

A mixture of 6.00 g (0.035 mole) of 1-(3-aminopropyl)-4-methylpiperazine and 6.97 g (0.043 mole) of 1,1'-carbonyldiimidazole in 400 ml of tetrahydrofuran was stirred at room temperature for 1 hr. A solution of 8.17 g (0.036 mole) of N-(2-phenylsulfonylethyl)-2-propanamine in 100 ml of tetrahydrofuran was added, and the mixture was refluxed for 16 hr. The solvent was removed in vacuo and the residue was partitioned between methylene chloride and water. The solution was dried over magnesium sulfate, and the solvent was removed in vacuo to give an oil. The oil was dissolved in methanol; a solution of two equivalents of maleic acid in methanol was added, and a white solid precipitated. This was collected to give 15.48 g (68.8%) of white crystalline solid; m.p. 162°-163° C. with decomposition.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04724235
출처 데이터셋uspto-grants-1988_02
ORD IDord-54b66e4802a3406cb2dc05cb341eaba1
출처 메모uspto-grants-1988_02