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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83606생성일: 2026년 10월 24일

1,2-Dichloroethane → (4-benzylpiperazin-1-yl)(1-(4-fluorobenzyl)-1H-indol-2-yl)methanone

https://huagongshe.com/ko/reaction/83606

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1-BenzylpiperazineHCID 75994—
반응물DiisopropylethylamineHCID 81531—
반응물1-(4-fluorobenzyl)-1H-indole-2-carboxylic acidHCID 18627069—
용매DimethylformamideHCID 6228—
용매Diethylether ethylacetateHCID 21584169—
생성물(4-benzylpiperazin-1-yl)(1-(4-fluorobenzyl)-1H-indol-2-yl)methanoneHCID 6657109671.7%

반응 단계

The following was added sequentially to anhydrous DMF: 1-(4-fluorobenzyl)-1H-indole-2-carboxylic acid (50 mg, 0.186 mmol), Hunig's Base (0.065 ml, 0.371 mmol), EDC (46.3 mg, 0.241 mmol), HOBT (37.0 mg, 0.241 mmol), and 1-benzylpiperazine (32.7 mg, 0.186 mmol). The solution was allowed to stir at room temperature for 22 h. At this time, a 1:1 solution of diethylether/ethyl acetate (5 mL) was added, and this was washed with aqueous 10% Na2CO3 (3×2 mL). The extract was then dried with anhydrous MgSO4, filtered, and the filtrate was concentrated in vacuo. The crude residue was purified by column chromatography (20 g silica, 80% EtOAC/Hexanes) to provide 57 mg of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846684B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-f9409ce4bfe340538e78425c0eebca35
출처 메모uspto-grants-2014_09