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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 648199생성일: 2026년 10월 25일

Potassium Iodide → 1-[4-(4-Benzo[d]isothiazol-3-yl-piperazin-1-yl)-butyl]-4,4-dimethyl-piperidine-2,6-dione

https://huagongshe.com/reaction/648199

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물3-(1-Piperazinyl)-1,2-benzisothiazoleHCID 2772144—
반응물1-(4-Bromobutyl)-4,4-dimethylpiperidine-2,6-dioneHCID 13660335—
용매AcetonitrileHCID 6342—
생성물1-[4-(4-Benzo[d]isothiazol-3-yl-piperazin-1-yl)-butyl]-4,4-dimethyl-piperidine-2,6-dioneHCID 1323249364%

반응 단계

A mixture of N-(4-bromobutyl)-3,3-dimethylglutarimide (4 g., 0.0145 mole) obtained according to the procedure of Example 9, 3-(1-piperazinyl)-1,2-benzisothiazole (3.18 g., 0.0145 mole), anhydrous potassium carbonate (20.04 g., 0.145 mole) and potassium iodide (0.25 g., 0.0015 mole) in 150 ml. of acetonitrile is stirred and refluxed for a period of 12 hr. The reaction mixture is filtered, concentrated in vacuo and residual material triturated with ether. Crystallization of the solid thus obtained from ether affords a 64% yield of analytically pure 1-[4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]butyl]-4,4-dimethyl-2,6-piperidinedione, m.p. 146°-147° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04411901
출처 데이터셋uspto-grants-1983_10
ORD IDord-5dc039cc55534781a6a3962d342d7d59
출처 메모uspto-grants-1983_10