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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7807생성일: 2026년 10월 23일

Cesium fluoride → (S)-2-[5-Naphthalen-1-yl-2-oxo-3-(4-trifluoromethylbenzoylamino)-2H-pyridin-1-yl]-3-phenylpropionic acid methyl ester

https://huagongshe.com/ko/reaction/7807

반응식

참여 물질

역할이름HCID투입량
반응물Cesium fluorideHCID 25953—
반응물1-Naphthaleneboronic acidHCID 254532—
반응물(S)-2-[5-Bromo-2-oxo-3-(4-trifluoromethylbenzoylamino)-2H-pyridin-1-yl]-3-phenylpropionic acid methyl esterHCID 69587645—
촉매HCID 178418851HCID 178418851—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물(S)-2-[5-Naphthalen-1-yl-2-oxo-3-(4-trifluoromethylbenzoylamino)-2H-pyridin-1-yl]-3-phenylpropionic acid methyl esterHCID 6958792681%

반응 단계

A mixture of (S)-2-[5-bromo-2-oxo-3-(4-trifluoromethylbenzoylamino)-2H-pyridin-1-yl]-3-phenylpropionic acid methyl ester from Step E (66.8 mg, 0.128 mmol), 1-naphthyleneboronic acid (44.0 mg, 0.256 mmol), cesium fluoride (97 mg, 0.64 mmol), tris(dibenzylideneacetone)dipalladium(0) chloroform complex (13.0 mg, 0.013 mmol) and bis(tri-t-butylphosphine)palladium(0) (16.0 mg, 0.031 mmol) in tetrahydrofuran (2.0 mL) was heated to reflux for 15 h. The reaction mixture was cooled to room temperature, diluted with diethyl ether (100 mL), washed with saturated ammonium chloride solution and brine. The organic layer was separated, dried with sodium sulfate, filtered and concentrated. Purification by medium pressure liquid chromatography on silica gel (1:5 ethyl acetate/hexanes) gave 59 mg (81%) of the title compound as a semisolid. MS 571.2 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087622B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-0a77d0470a194567bea60da99ff1e7cf
출처 메모uspto-grants-2006_08