돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 327929생성일: 2026년 10월 26일

Acetic Acid → N-(2'-(4"-Hydroxyphenyl)ethyl)-3-methoxyestra-1,3,5(10)-triene-17beta-amine

https://huagongshe.com/reaction/327929

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물TyramineHCID 5610—
반응물TetrahydrofuranHCID 8028—
반응물(+)-Estrone 3-methyl etherHCID 92895—
용매MethanolHCID 887—
용매Ethyl AcetateHCID 8857—
생성물N-(2'-(4"-Hydroxyphenyl)ethyl)-3-methoxyestra-1,3,5(10)-triene-17beta-amineHCID 18638571—

반응 단계

Tyramine (5.27 g), glacial acetic acid (5.27 g), estrone methyl ether (4.92 g) sodium cyanoborohydride (1.09 g), tetrahydrofuran (43 ml) were added to methanol (58 ml). The reacting mixture was allowed to stir for 21 hours at room temperature. TLC (ethyl acetate) revealed the formation of a more polar product (Rf 0.25). After 19 hours TLC revealed that the starting material still remained in the reaction solution. The system was warmed at 40° C. in an oil bath. The solution remained as a white undissolved solid. After 29 hours the system was allowed to reach room temperature. Excess solvent was removed under reduced pressure. Water was added and made basic (pH 9) with aqueous 50% NAOH. The white solid did not dissolve in ether and was slightly soluble in ethyl acetate. The solid was filtered and mixed with 34 g of flash silica gel and ethyl acetate. The solvent was removed under reduced pressure. The silica gel was poured on top of the chromatographic column, The compound was eluted with ethyl acetate. Solid was obtained and was recrystallized from ethyl acetate, mp 184°-185° C. (diabetes)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05274089
출처 데이터셋uspto-grants-1993_12
ORD IDord-26d0002434ab49208f75f6551bd4469e
출처 메모uspto-grants-1993_12