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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83681생성일: 2026년 10월 26일

1,2-Dichloroethane → N-benzyl-1-(1-(4-chlorobenzyl)-7-methyl-1H-indole-2-carbonyl)piperidine-4-carboxamide

https://huagongshe.com/reaction/83681

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물N-benzylpiperidine-4-carboxamideHCID 3868064—
반응물1-(4-chlorobenzyl)-7-methyl-1H-indole-2-carboxylic acidHCID 68379759—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-benzyl-1-(1-(4-chlorobenzyl)-7-methyl-1H-indole-2-carbonyl)piperidine-4-carboxamideHCID 66571684—

반응 단계

The following was added to sequentially to DMF (2 mL): 1-(4-chlorobenzyl)-7-methyl-1H-indole-2-carboxylic acid (50 mg, 0.167 mmol), DIPEA (0.10 mL, 0.584 mmol), EDC (38 mg, 0.200 mmol), and HOBT (31 mg, 0.200 mmol). This was allowed to stir for 30 min at rt, after which time the crude N-benzylpiperidine-4-carboxamide (˜36 mg, 0.20 mmol) was added. The reaction was stirred at rt for 18 h, at which time the reaction was diluted with 1:1 EtOAc:diethyl ether and washed with 10% aq. sodium carbonate (2×), dried over magnesium sulfate, and concentrated. The residue was purified via silica gel flash chromatography (20 g silica, 50% EtOAc/Hexanes) to afford the title compound as a white powder. (Yield: 39 mg, 0.078 mmol, 47%) 1H NMR (400 MHz, CDCl3) 7.50, 7.38-7.26, 7.18, 7.05-6.97, 6.81, 6.63, 5.72, 5.66-5.57, 4.70-3.89, 4.44, 2.86-2.66, 2.57, 2.32-2.23, 1.77

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846684B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-add255bcb05444f6877328775a1193d3
출처 메모uspto-grants-2014_09