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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 601782생성일: 2026년 10월 25일

3-Methoxypyridine → 5-Chloro-3-hydroxy-3-(3-methoxy-pyridin-4-yl)-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/601782

반응식

참여 물질

역할이름HCID투입량
반응물3-MethoxypyridineHCID 23719—
반응물2-BromomesityleneHCID 68473—
반응물5-chloro-1H-indole-2,3-dioneHCID 87203—
반응물HCID 178418306HCID 178418306—
용매PentaneHCID 8003—
용매TetrahydrofuranHCID 8028—
생성물5-Chloro-3-hydroxy-3-(3-methoxy-pyridin-4-yl)-1,3-dihydro-indol-2-oneHCID 57517882—

반응 조건

온도-78 °C

반응 단계

A 1.7 M solution of tert-butyllithium in pentane (57.8 mL) was added to THF (200 ml) at −78° C. 2-Bromomesitylene (3.6 mL) was added dropwise, keeping the temperature below −60° C., and the mixture stirred at −78° C. for 1 h. 3-Methoxypyridine (3.6 mL) was added dropwise at −78° C. and then the mixture was allowed to warm to −5° C. over 2 h. The reaction mixture was re-cooled to −78° C. and a slurry of 5-chloroisatin (3.26 g) in THF (100 mL) was added portionwise keeping the temperature below −60° C. The reaction mixture was stirred at −78° C. for 1 h. The cooling bath was removed and the reaction mixture was stirred for 30 min. The reaction mixture was quenched with 10% aqueous ammonium chloride solution and extracted several times with ethyl acetate. The combined organic layers were washed with water, dried over magnesium sulfate and evaporated to low volume. Upon standing, 0.73 g of a pale yellow solid separated which was filtered off, washed with ethyl acetate and dried in vacuo.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902379B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-7358de44a10043df925ab82ea77fdd1a
출처 메모uspto-grants-2011_03