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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1084768생성일: 2026년 10월 25일

Phenol → 1,3-dihydro-1-(propyl-4-pyridinylamino)-2H-indol-2-one

https://huagongshe.com/reaction/1084768

반응식

참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물Sodium HydroxideHCID 14798—
반응물4-Bromopyridinium chlorideHCID 88100—
반응물1-(Propylamino)-oxindoleHCID 15703628—
생성물1,3-dihydro-1-(propyl-4-pyridinylamino)-2H-indol-2-oneHCID 1499426114.4%

반응 단계

To a stirred solution of 1-(propylamino)-oxindole (10.4 g) and phenol (30.8 g), preheated to 150° C. under nitrogen, was added 4-bromopyridine hydrochloride (11.04 g) over 5 min. Heating was continued for 7 hours at which time the reaction mixture was cooled to room temperature and made basic by slow addition of dilute aqueous sodium hydroxide. The product was extracted four times with ethyl acetate and the combined organic layers back-extracted with dilute aqueous sodium hydroxide, washed with brine, and dried (K2CO3). Filtration and concentration gave the crude product. Purification via flash column chromatography (silica gel, EtOAc), preparative high performance liquid chromatography (HPLC) (silica gel, EtOAc→2% Et3N/0-7% MeOH/EtOAc), and a third column (alumina, EtOAc) followed. Recrystallization from ethyl acetate-pentane afforded 2.10 g (14%) of 1,3-dihydro-1-(propyl-4-pyridinylamino)-2H-indol-2-one, as a solid, m.p. 140°-143° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05006537
출처 데이터셋uspto-grants-1991_04
ORD IDord-e5647d7bd11f446b87ff1d99d29f7409
출처 메모uspto-grants-1991_04