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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1164985생성일: 2026년 10월 26일

Triethylamine → Methyl 2-[2-Hydroxy-3-[N-[2-[N-(phenylaminocarbonyl)amino]ethyl]amino]propoxy]benzoate

https://huagongshe.com/reaction/1164985

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methyl 2-(oxiran-2-ylmethoxy)benzoateHCID 279510—
반응물3-(2-Aminoethyl)-1-phenylurea hydrochlorideHCID 19863750—
용매MethanolHCID 887—
생성물Methyl 2-[2-Hydroxy-3-[N-[2-[N-(phenylaminocarbonyl)amino]ethyl]amino]propoxy]benzoateHCID 130309447.5%

반응 단계

4.8 g of N-phenyl-N'-(2-aminoethyl)urea HCl salt (0.024 mole) was placed in 100 ml of methanol, and 2.5 g of triethylamine (0.024 mole) was added. While this reaction mixture was being stirred, a solution of 5 g of methyl 2-(2,3-epoxypropoxy)benzoate (0.024 mole) in 25 ml methanol was added slowly. The solution was then heated to reflux for 4 hours. The methanol was removed under reduced pressure and the resulting gel-like solid was dissolved in 100 ml of methylene chloride. The organic layer was washed twice with 100 ml of water and dried over anhydrous magnesium sulfate. Removal of the methylene chloride left an oil which was dissolved in 50 ml of methanol/ethyl ether (1:1) from which the product crystallized slowly upon refrigeration to afford 0.7 g (7.5%) of product having a melting point of 133°-134° C. The compound was identified by its NMR spectrum and elemental analysis.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04906661
출처 데이터셋uspto-grants-1990_03
ORD IDord-c10f3505907744b89d2b71a5cc55d86d
출처 메모uspto-grants-1990_03