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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 601765생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/601765

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-2-yl)-1,3-dihydro-indol-2-oneHCID 57517760—

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 stirred between −30° C. and −20° C. 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, 1.05 g of a cream-colored 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-147a4bc83edf47938af5cb28e064f44c
출처 메모uspto-grants-2011_03