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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 369035생성일: 2026년 10월 26일

Sodium Carbonate → 6-(4-Carboxyphenyl)-8-methoxy-1,7-naphthyridine

https://huagongshe.com/reaction/369035

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물4-Carboxyphenylboronic AcidHCID 312183—
반응물6-Trifluoromethylsulfonyloxy-8-methoxy-1,7-naphthyridineHCID 23284635—
촉매Tri-o-tolylphosphineHCID 80271—
촉매1,5-Diphenylpenta-1,4-dien-3-one;palladiumHCID 154270—
용매DimethylformamideHCID 6228—
생성물6-(4-Carboxyphenyl)-8-methoxy-1,7-naphthyridineHCID 2328464280.8%

반응 단계

To a solution of 6-trifluoromethylsulfonyloxy-8-methoxy-1,7-napthyridine (1.5 g, 4.86 mmol) in DMF (40 ml) is added 4-carboxy-phenylboronic acid (0.866 g, 5.34 mmol), bis(dibenzylidenacetone) palladium (112 mg, 0.167 mmol), tri-o-tolylphosphine (96 mg, 0.32 mmol) and aqueous Na2CO3 (14.6 ml, 2N,). The reaction mixture is stirred at 110° for 3 h. The hot solution is filtred through cellit and the solution evaporated to dryness. The crude product is dissolved in hot water (60 ml) and the water phase washed with ethyl acetate (3×50 ml). The product is precipitated from the water phase by carefully adding aqueous HCl (2N, 6 ml). The suspension is filtered and the crude product is stirred again in hot ethyl acetate (50 ml). The cold suspension is filtered to yield the title compound (1.10 g). M+280; Melting point >300°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06136821
출처 데이터셋uspto-grants-2000_10
ORD IDord-449fc1ba55304cbb90163e63a52ba620
출처 메모uspto-grants-2000_10