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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83684생성일: 2026년 10월 25일

Diisopropylethylamine → N-benzyl-1-(1-(4-chlorobenzyl)-3-methyl-1H-indole-2-carbonyl)piperidine-4-carboxamide

https://huagongshe.com/reaction/83684

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물N-benzylpiperidine-4-carboxamideHCID 3868064—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물1-(4-chlorobenzyl)-3-methyl-1H-indole-2-carboxylic acidHCID 68379742—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-benzyl-1-(1-(4-chlorobenzyl)-3-methyl-1H-indole-2-carbonyl)piperidine-4-carboxamideHCID 66571685—

반응 단계

The following was added to sequentially to DMF (3 mL): 1-(4-chlorobenzyl)-3-methyl-1H-indole-2-carboxylic acid (90 mg, 0.315 mmol), DIPEA (0.170 mL, 0.945 mmol), and HATU (144 mg, 0.378 mmol). This was allowed to stir for 30 min at rt, after which time the crude N-benzylpiperidine-4-carboxamide (˜70 mg, 0.315 mmol) was added. The reaction was stirred at rt for 17 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 an oil. Yield: (77 mg, 0.153 mmol, 51%) 1H NMR (400 MHz, CDCl3) 7.59, 7.34-7.14, 7.03, 5.73, 5.57, 5.43-5.32, 4.76, 4.43, 3.77-3.64, 3.10, 2.80, 2.19-1.52

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846684B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-3d24471df73c4188ab81f0d26204cecc
출처 메모uspto-grants-2014_09