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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 56980생성일: 2026년 10월 24일

Diisopropylcarbodiimide → 4-({2-[5-Chloro-4-(5-chloro-2-cyanophenyl)-2-oxopyridin-1(2H)-yl]propanoyl}amino)-2-fluorobenzoic acid

https://huagongshe.com/ko/reaction/56980

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylcarbodiimideHCID 12734—
반응물4-Amino-2-fluorobenzoic acidHCID 302680—
반응물2-[5-Chloro-4-(5-chloro-2-cyanophenyl)-2-oxopyridin-1(2H)-yl]propanoic acidHCID 117622549—
용매1,1-DichloroethaneHCID 6365—
생성물4-({2-[5-Chloro-4-(5-chloro-2-cyanophenyl)-2-oxopyridin-1(2H)-yl]propanoyl}amino)-2-fluorobenzoic acidHCID 117622831—

반응 단계

Under argon and at RT, 37 mg (0.30 mmol, 1.0 eq.) of N,N′-diisopropylcarbodiimide were added to a solution of 100 mg (0.30 mmol) of 2-[5-chloro-4-(5-chloro-2-cyanophenyl)-2-oxopyridin-1(2H)-yl]propanoic acid (racemate) (Example 12.1D) in 2 ml of dichloroethane, the mixture was stirred for 10 min, 46 mg (0.30 mmol) of 4-amino-2-fluorobenzoic acid were added and the mixture was stirred under reflux overnight. Subsequently, the reaction mixture was concentrated under reduced pressure and the crude product was purified by preparative HPLC (Reprosil C18, water/methanol gradient). Yield: 41 mg (29% of theory)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434690B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-c9c2dcbfee0b4bc0b394f923bc0eaf8b
출처 메모uspto-grants-2016_09