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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83613생성일: 2026년 10월 24일

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → N-(3-chlorobenzyl)-1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxamide

https://huagongshe.com/ko/reaction/83613

반응식

참여 물질

역할이름HCID투입량
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물Benzenemethanamine, 3-chloro-HCID 77802—
반응물DiisopropylethylamineHCID 81531—
반응물1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxylic acidHCID 57385796—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물N-(3-chlorobenzyl)-1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxamideHCID 57385554—

반응 단계

1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxylic acid (336 mg, 0.847 mmol), 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (203 mg, 1.509 mmol), and 1-Hydroxybenzotriazole (143 mg, 1.059 mmol) were dissolved in 2.0 mL of DCM. The reaction was allowed to stir for 10 minutes before N,N-Diisopropylethylamine (185 μL, 1.059 mmol) and (3-chlorophenyl)methanamine (100 mg, 0.706 mmol) were added as a 1.0 mL DCM solution. The reaction was allowed to stir overnight. The reaction was diluted with water and ethyl acetate. The layers were separated and the organic layer was washed with another aliquot of water. The ethyl acetate layer was washed with 1N HCl followed by saturated sodium bicarbonate then saturated sodium chloride. The organic layer was dried over magnesium sulfate, filtered and concentrated. The crude material was triturated with methanol and filtered under vacuum to obtain pure product as a white solid. Yield: 179 mg (White solid)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846684B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-71ed657745f44f92a3d0774905bfaea8
출처 메모uspto-grants-2014_09