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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 340417생성일: 2026년 10월 23일

1-Hydroxybenzotriazole → HCID 66589583, 화합물

https://huagongshe.com/ko/reaction/340417

반응식

참여 물질

역할이름HCID투입량
반응물1-HydroxybenzotriazoleHCID 75771—
반응물5-Hydroxyindole-2-carboxylic acidHCID 88958—
반응물1-Benzyl-4-piperidylamineHCID 415852—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매DimethylformamideHCID 6228—
용매TriethylamineHCID 8471—
생성물HCID 66589583HCID 6658958324%

반응 단계

To a stirred mixture of 5-hydroxy-1H-indole-2-carboxylic acid (1.85 g, 10.43 mmol) in anhydrous dimethylformamide (15 mL) was added triethylamine (1.73 mL), 1-hydroxybenzotriazole (1.64 g), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (2.39 g) and 1-benzylpiperidin-4-ylamine (2.39 g, 12.54 mmol). The reaction mixture was stirred at room temperature over-night and then solvents were removed under reduced pressure, poured into water, filter the solid and washed with water. The solid was purified by silica gel column chromatography, eluted with CH2Cl2:MeOH (93:7) to afford 0.87 g (24%) of N-(1-benzylpiperidin-4-yl)-5-hydroxy-1H-indole-2-carboxamide as a white solid. 1H NMR (DMSO-d6, 300 MHz): δ 11.17 (s, 1H), 8.72 (s, 1H), 8.07 (d, J=7.8 Hz, 1H), 7.7.29 (m, 6H), 6.91 (s, 1H), 6.82 (s, 1H), 6.68 (m, 1H), 3.75 (br s, 1H), 3.46 (s, 2H), 2.81 (d, J=11.4 Hz, 2H), 2.02 (t, J=10.8 Hz, 2H), 1.77 (m, 2H), 1.56 (m, 2H); LCMS (m/z): 350 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895578B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-075012a4c6ba42229ec6dc377d676493
출처 메모uspto-grants-2014_11