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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1673719생성일: 2026년 10월 26일

Tributylphosphine → 4'-({4-Butyl-1-[(5-chloro-1-benzothien-3-yl)methyl]-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl}methyl)biphenyl-2-carbonitrile

https://huagongshe.com/reaction/1673719

반응식

참여 물질

역할이름HCID투입량
반응물TributylphosphineHCID 13831—
반응물1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
반응물5-Chlorobenzo[b]thiophene-3-methanolHCID 2776136—
반응물4'-[(4-Butyl-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl)methyl]biphenyl-2-carbonitrileHCID 135401222—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물4'-({4-Butyl-1-[(5-chloro-1-benzothien-3-yl)methyl]-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl}methyl)biphenyl-2-carbonitrileHCID 5748013355%

반응 단계

A mixture of 4′-[(4-butyl-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl)methyl]biphenyl-2-carbonitrile (1 g), 1,1′-(azodicarbonyl)dipiperidine (1.41 g), tributylphosphine (1.56 mL), (5-chloro-1-benzothien-3-yl)methanol (0.83 g) and tetrahydrofuran (50 mL) was stirred at room temperature for 4 hr. The reaction mixture was diluted with ethyl acetate, washed with 1 M hydrochloric acid and then with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography to give the title compound as a colorless solid (0.82 g, 55%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07998968B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-111467a92c42469889c40f7df985eaf2
출처 메모uspto-grants-2011_08