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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1436199생성일: 2026년 10월 26일

Ethylene Glycol → (S)-3-chloro-N-(4-hydroxy-1-(4-(1-methyl-2-(2-methyl-1,3-dioxolan-2-yl)-1H-imidazol-4-yl)phenyl)butan-2-yl)-4-isopropoxybenzamide

https://huagongshe.com/reaction/1436199

반응식

참여 물질

역할이름HCID투입량
반응물Ethylene GlycolHCID 174—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물(S)-N-(1-(4-(2-acetyl-1-methyl-1H-imidazol-4-yl)phenyl)-4-hydroxybutan-2-yl)-3-chloro-4-isopropoxybenzamideHCID 57594136—
용매BenzeneHCID 241—
생성물(S)-3-chloro-N-(4-hydroxy-1-(4-(1-methyl-2-(2-methyl-1,3-dioxolan-2-yl)-1H-imidazol-4-yl)phenyl)butan-2-yl)-4-isopropoxybenzamideHCID 5759471316%

반응 조건

온도70 °C

반응 단계

150 mg (0.31 mmol) of (S)-N-(1-(4-(2-acetyl-1-methyl-1H-imidazol-4-yl)phenyl)-4-hydroxybutan-2-yl)-3-chloro-4-isopropoxybenzamide in 2 mL of benzene was treated with 34.6 uL (0.62 mmol) of ethane-1,2-diol and 59 mg (0.31 mmol) of p-toluenesulfonic acid monohydrate. The reaction was stirred at 70° C. for 2 h after which the solvents were evaporated and the residue purified via reverse phase HPLC (acetonitrile/water). 25.5 mg (16% yield) of 4 was obtained and characterized by LCMS and HNMR.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07618981B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-ffcab30a72144937a3d156aeefaad9e6
출처 메모uspto-grants-2009_11