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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 359034생성일: 2026년 10월 25일

Dimethylformamide → 4-[1-(2-chlorophenyl)-1H-indazol-3-yl]-1-piperazine carboxamide

https://huagongshe.com/reaction/359034

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Diisopropyl EtherHCID 7914—
반응물NitroureaHCID 62372—
반응물1-(2-chlorophenyl)-3-(1-piperazinyl)-1H-indazoleHCID 15117079—
용매WaterHCID 962—
생성물4-[1-(2-chlorophenyl)-1H-indazol-3-yl]-1-piperazine carboxamideHCID 1511710144.5%

반응 단계

A mixture of 7.9 g of 1-(2-chlorophenyl)-3-(1-piperazinyl)-1H-indazole, 7.3 g of nitrourea and 100 ml of dimethylformamide was heated on a steam bath for 15 minutes. The reaction mixture was diluted with water and extracted with ethyl acetate. The extract was washed with water, dried over anhydrous magnesium sulfate and concentrated. The concentrate was flash chromatographed on silica gel eluting with chloroform/methanol (5%). Concentration of the appropriate fraction yielded a foam, which when stirred overnight with isopropyl ether afforded 4.0 g of 4-[1-(2-chlorophenyl)-1H-indazol-3-yl]-1-piperazine carboxamide as a powder. A 3.4 g sample of the free base was dissolved in diethyl ether and treated with 1.1 g of fumaric acid. The resulting salt was recrystallized from ethyl acetate to yield 2.3 g (22%) of 4-[1-(2-chlorophenyl)-1H-indazol-3-yl]-1-piperazine carboxamide hemifumarate, m.p. 156°-158°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04999356
출처 데이터셋uspto-grants-1991_03
ORD IDord-de53b221082b433690531e16aba7a050
출처 메모uspto-grants-1991_03