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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4555생성일: 2026년 10월 23일

2-((4-(2-(Cyclopropylmethoxy)ethyl)phenoxy)methyl)oxirane → 1-[N-[2-(3-carbamoyl-4-hydroxy-phenoxy)-ethyl]-benzylamino]-3-[4-[2-(cyclopropylmethoxy)ethyl]-phenoxy]-2-propanol

https://huagongshe.com/ko/reaction/4555

반응식

참여 물질

역할이름HCID투입량
반응물2-((4-(2-(Cyclopropylmethoxy)ethyl)phenoxy)methyl)oxiraneHCID 11791542—
반응물5-(2-Benzylaminopropoxy)salicylamideHCID 13754334—
용매IsopropanolHCID 3776—
생성물1-[N-[2-(3-carbamoyl-4-hydroxy-phenoxy)-ethyl]-benzylamino]-3-[4-[2-(cyclopropylmethoxy)ethyl]-phenoxy]-2-propanolHCID 20151321—

반응 단계

A solution of 14.3 g of 1-[2-(cyclopropyl-methoxy)ethyl]-4-(2,3-epoxypropoxy)-benzene (German Offenlegungsschrift No. 2,649,605) and 16.3 g of 5-[2-(benzylamino)propoxy]-salicylamide in 200 ml of isopropanol is refluxed for 18 hours. The reaction mixture is concentrated by evaporation to leave crude 1-[N-[2-(3-carbamoyl-4-hydroxy-phenoxy)-ethyl]-benzylamino]-3-[4-[2-(cyclopropylmethoxy)ethyl]-phenoxy]-2-propanol in the form of brown oil, which can be further processed without additional purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727067
출처 데이터셋uspto-grants-1988_02
ORD IDord-b95195d2cd784a148d1234c8bc6ee701
출처 메모uspto-grants-1988_02