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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46146생성일: 2026년 10월 23일

Benzonitrile, 4-bromo- → HCID 178461988, 화합물

https://huagongshe.com/ko/reaction/46146

반응식

참여 물질

역할이름HCID투입량
반응물Benzonitrile, 4-bromo-HCID 12162—
반응물Binap, (A+-)-HCID 634876—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물HCID 178435110HCID 178435110—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물HCID 178461988HCID 178461988—

반응 조건

온도95 °C

반응 단계

To a mixture of 2-((S)-1-(2-fluorophenyl)ethylamino)-5-methylthiazol-4(5H)-one (0.0500 g, 0.198 mmol), 4-bromobenzonitrile (Aldrich, 0.0721 g, 0.396 mmol), Pd2(dba)3 (Aldrich, 0.0127 g, 0.0139 mmol), 2-(diphenylphosphino)-1-(2-(diphenylphosphino)naphthalen-1-yl)naphthalene (Strem, 0.0123 g, 0.0198 mmol), and NaN(TMS)2 (Aldrich, 0.0727 g, 0.396 mmol) was added toluene (2 mL) in a dry box. The mixture was gradually heated to 95° C. and stirred overnight. The reaction was cooled to ambient temp. and quenched with NH4Cl (5 mL). The reaction mixture was extract with EtOAc. The organic phase was dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography. MS: 354 (M+1)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541592B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-186e9403d5944feca041a124aeb48779
출처 메모uspto-grants-2013_09