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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83633생성일: 2026년 10월 24일

2-(4-Chlorophenyl)ethylamine → HCID 66571402, 화합물

https://huagongshe.com/ko/reaction/83633

반응식

참여 물질

역할이름HCID투입량
반응물2-(4-Chlorophenyl)ethylamineHCID 67430—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxylic acidHCID 57385796—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물HCID 66571402HCID 66571402—

반응 단계

1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxylic acid (100 mg, 0.252 mmol), N1-((ethylimino)methylene)-N3,N3-dimethylpropane-1,3-diamine hydrochloride (72.5 mg, 0.378 mmol), and 1H-benzo[d][1,2,3]triazol-1-ol (51.1 mg, 0.378 mmol) were dissolved in DCM (Volume: 3.0 mL). The reaction was stirred for 10 minutes before 2-(4-chlorophenyl)ethanamine (0.053 mL, 0.378 mmol) and N-ethyl-N-isopropylpropan-2-amine (0.066 mL, 0.378 mmol). The reaction was stirred overnight at room temperature. The reaction was diluted with water and ethyl acetate. The organic layer was washed with 1N HCl, saturated sodium bicarbonate solution, and finally saturated sodium chloride. the organic layer was then dried over magnesium sulfate, filtered and concentrated. The crude material was triturated in ethyl acetate to give the product as a white solid. (Yield: 60 mg, white solid) 1H-NMR (400 MHz, DMSO-d6) 7.85, 7.63, 7.54, 7.38-7.31, 7.24-7.18, 7.14-7.06, 6.71, 5.49, 4.37, 4.00, 3.26, 2.92, 2.69, 2.37-2.27, 1.76-1.22

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846684B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-36bf2828d2b24b7dbdd48dec96b99eb0
출처 메모uspto-grants-2014_09