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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1752942생성일: 2026년 10월 24일

1,2-Dichloroethane → (R)-(3-((1-(5'-chloro-2'-fluoro-[1,1-biphenyl]-4-yl)-4-ethoxy-4-oxobutan-2-yl)amino)-3-oxopropyl)phosphonic acid

https://huagongshe.com/ko/reaction/1752942

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물3-Phosphonopropionic acidHCID 1682—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물HCID 59607661HCID 59607661—
용매DimethylformamideHCID 6228—
생성물(R)-(3-((1-(5'-chloro-2'-fluoro-[1,1-biphenyl]-4-yl)-4-ethoxy-4-oxobutan-2-yl)amino)-3-oxopropyl)phosphonic acidHCID 9033170211.8%

반응 단계

(R)-ethyl 3-amino-4-(5′-chloro-2′-fluoro-[1,1-biphenyl]-4-yl)butanoate (114 mg, 0.306 mmol), 3-phosphonoproprionic acid (47.2 mg, 0.306 mmol), EDC (58.7 mg, 0.306 mmol) and HOBT (46.9 mg, 0.306 mmol) were mostly dissolved in DMF (1 mL), and DIPEA (0.321 mL, 1.837 mmol) was added. The reaction mixture was stirred and heated at 70° C. approximately 18 hours, then filtered and purified by HPLC: 30-80% ACN/H2O 0.1% TFA, 40 mL/min over 15 min 30×100 Sunfire C18, product elutes approximately 5.5-8 min. A mixed fraction was repurified on a 20-55% gradient over 20 min, and product eluted ˜12.5-13 min. The fractions were evaporated to dryness to afford (R)-(3-((1-(5′-chloro-2′-fluoro-[1,1-biphenyl]-4-yl)-4-ethoxy-4-oxobutan-2-yl)amino)-3-oxopropyl)phosphonic acid (17 mg) LCMS (ES+) C21H24ClFNO6P: Calc.: 471.1; Found: 472.0[M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09163040B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-0bb2365961004c3b8ad64fa1862f09ee
출처 메모uspto-grants-2015_10