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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 129057생성일: 2026년 10월 24일

2-(Chloromethyl)-4-isopropyl-6-methoxybenzo[D]isothiazol-3(2H)-one 1,1-dioxide → HCID 15293148, 화합물

https://huagongshe.com/ko/reaction/129057

반응식

참여 물질

역할이름HCID투입량
반응물2-(Chloromethyl)-4-isopropyl-6-methoxybenzo[D]isothiazol-3(2H)-one 1,1-dioxideHCID 9995173—
반응물HCID 19373059HCID 19373059—
반응물Potassium tert-butoxideHCID 23665647—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물HCID 15293148HCID 1529314847.1%

반응 단계

A mixture of 3-(4-morpholinylmethyl)pyrido[1,2-a]pyrimidine-2,4-dione hydrochloride (0.6 g) and potassium t-butoxide (0.49 g) in dimethylformamide (20 mL) was stirred at room temperature for five minutes. 2-Chloromethyl-4-isopropyl-6-methoxysaccharin (0.61 g) was added and stirring was continued at room temperature for one hour. The reaction mixture was diluted with water (50 mL) and extracted with dichloromethane (3×200 mL). The dichloromethane extract was dried over sodium sulfate and stripped of volatiles, finally under high vacuum. The crude product (780 mg) was combined with that (0.65 g) from another run at the same scale using sodium hydride (60% dispersion in mineral oil, 0.19 g) instead of potassium t-butoxide and purified by column chromatography on silica gel with dichloromethane-methanol (95:5) as eluant affording 2-[3-(4-morpholinylmethyl)-4-oxo-4-H-pyrido[1,2-a]pyrimidin-2yl]oxymethyl-4-isopropyl-6-methoxysaccharin (500 mg, 23% yield), part of which was recrystallized from ethanol (m.r. 177°-180° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05466701
출처 데이터셋uspto-grants-1995_11
ORD IDord-a730856b16544f22a7170539fafd9946
출처 메모uspto-grants-1995_11