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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 56679생성일: 2026년 10월 24일

Benzoic acid, 4-amino-, 1,1-dimethylethyl ester → tert-Butyl 4-{[2-{4-[5-chloro-2-(trifluoromethyl)phenyl]-2-oxopyridin-1(2H)-yl}-3-(pyridin-3-yl)propanoyl]amino}benzoate

https://huagongshe.com/ko/reaction/56679

반응식

참여 물질

역할이름HCID투입량
반응물Benzoic acid, 4-amino-, 1,1-dimethylethyl esterHCID 233272—
반응물2-{4-[5-Chloro-2-(trifluoromethyl)phenyl]-2-oxopyridin-1(2H)-yl}-3-(pyridin-3-yl)propanoic acidHCID 117622751—
용매DimethylformamideHCID 6228—
생성물tert-Butyl 4-{[2-{4-[5-chloro-2-(trifluoromethyl)phenyl]-2-oxopyridin-1(2H)-yl}-3-(pyridin-3-yl)propanoyl]amino}benzoateHCID 117622696—

반응 단계

26 mg (purity 92%, 0.06 mmol) of 2-{4-[5-chloro-2-(trifluoromethyl)phenyl]-2-oxopyridin-1(2H)-yl}-3-(pyridin-3-yl)propanoic acid (racemate) and 1.1 eq. of tert-butyl 4-aminobenzoate were reacted according to General Method 5A. The reaction mixture was freed from DMF and the residue was stirred with ice-water. The crystals obtained were filtered off, washed with water and dried under reduced pressure. Yield: 33 mg (purity 94%, 92% of theory)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434690B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-c70f8d423f4a4954bde2b7ce414da183
출처 메모uspto-grants-2016_09