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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 229109생성일: 2026년 10월 26일

Methyl Acetate → (r)-2-(3-{3-[[3-(Trifluoromethyl)-4-fluoro-benzyl](2,2-diphenylethyl)amino]-1-methyl-propoxy}-phenyl)acetic acid hydrochloride salt

https://huagongshe.com/reaction/229109

반응식

참여 물질

역할이름HCID투입량
반응물Methyl AcetateHCID 6584—
반응물4-Fluoro-3-(trifluoromethyl)benzaldehydeHCID 522269—
반응물2-Chloro-3-(trifluoromethyl)benzaldehydeHCID 2736672—
반응물Ether hydrochlorideHCID 10953452—
반응물(R)-2-(3-{3-[(2,2-diphenylethyl)amino]-1-methyl-propoxy}phenyl)acetic acidHCID 68864815—
용매Diethyl EtherHCID 3283—
생성물(r)-2-(3-{3-[[3-(Trifluoromethyl)-4-fluoro-benzyl](2,2-diphenylethyl)amino]-1-methyl-propoxy}-phenyl)acetic acid hydrochloride saltHCID 68864196—

반응 단계

Following the procedure of Example 7(d) except (R)-2-(3-{3-[(2,2-diphenylethyl)amino]-1-methyl-propoxy}-phenyl)acetic acid and 3-(trifluoromethyl)-4-fluoro-benzaldehyde were used instead of (R)-2-(3-{3-(2,2-diphenylethyl)amino]-3-methyl-propoxy}phenyl)acetic acid methyl ester and 2-chloro-3-trifluoromethylbenzaldehyde in step (d) the corresponding carboxylic acid was obtained. The crude product was purified by preparative HPLC (TMC CombiPrep PDS, 75×30 mm, 25 mL/min, acetonitrile: H2O, UV detection at 254 nm) to afford the free base. The resulting amine/carboxylic acid was dissolved in Et2O (diethylether) and acidified with 1.0 M HCl/Et2O. The reaction mixture was concentrated in vacuo and dried under reduced pressure to give the title compound as a white solid, 95 mg (88%). MS (ESI) 580.6 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560586B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-04f1056c8c994635b795ee80ded4a5ce
출처 메모uspto-grants-2009_07