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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 657728생성일: 2026년 10월 27일

1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) → 2-(4-methoxy-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)-5-methylbenzonitrile

https://huagongshe.com/reaction/657728

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
반응물2-Bromo-5-methylbenzonitrileHCID 12557201—
반응물Sodium t-butoxideHCID 23676156—
반응물4-methoxy-5H,6H,7H,8H-pyrido[4,3-d]pyrimidineHCID 50989214—
촉매(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
생성물2-(4-methoxy-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)-5-methylbenzonitrileHCID 59840712—

반응 단계

A 100 mL flask was charged with 4-methoxy-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine (2.78 g, 16 mmol), 2-bromo-5-methylbenzonitrile (4.18 g, 19.2 mmol), bis(dibenzylideneacetone)palladium(0) (372 mg, 0.64 mmol), xantphos (529 mg, 0.896 mmol), and sodium tert-butoxide (2.33 g, 24 mmol), capped with a septum and purged with nitrogen. Dry argon-sparged toluene (50 mL) was added. The heterogeneous mixture was placed in an oil bath at 100° C., and heated under argon overnight. After 14 hours, TLC showed the reaction was complete. The mixture was removed from the heat, diluted with ethyl acetate (50 mL), filtered and concentrated in vacuo. The residue was purified by silica gel column (0-100% EtOAc/hexane) to afford a light orange solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08076345B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-21cd55d605a647a0bbd887eacb573e8f
출처 메모uspto-grants-2011_12