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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 344385생성일: 2026년 10월 26일

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → N-(5-(4-(4-amino-5-chloro-2-methoxybenzoylaminomethyl)piperidin-1-yl)pentyl)-1-methyl-1 H-indazole-3-carboxamide

https://huagongshe.com/reaction/344385

반응식

참여 물질

역할이름HCID투입량
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1H-Indazole-3-carboxylic acid, 1-methyl-HCID 689105—
반응물4-Amino-N-(1-(5-aminopentyl)piperidin-4-ylmethyl)-5-chloro-2-methoxybenzamideHCID 54008363—
용매DimethylformamideHCID 6228—
생성물N-(5-(4-(4-amino-5-chloro-2-methoxybenzoylaminomethyl)piperidin-1-yl)pentyl)-1-methyl-1 H-indazole-3-carboxamideHCID 5374630026.7%

반응 조건

온도0 °C

반응 단계

4-Amino-N-(1-(5-aminopentyl)piperidin-4-ylmethyl)-5-chloro-2-methoxybenzamide (0.53 g) was dissolved in dimethylformamide (20 ml). 1-Methylindazole-3-carboxylic acid (0.27 g) and 1-hydroxybenzotriazole (0.25 g) were added, and the mixture was stirred at 0° C. for 15 min. Then, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (0.35 g) was added, and the mixture was stirred at room temperature for 16 hr. The reaction mixture was concentrated under reduced pressure. Aqueous potassium carbonate solution was added to the residue and the mixture was extracted with ethyl acetate. The extract was dried over magnesium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography to give 0.20 g of N-(5-(4-(4-amino-5-chloro-2-methoxybenzoylaminomethyl)piperidin-1-yl)pentyl)-1-methyl-1 H-indazole-3-carboxamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05864039
출처 데이터셋uspto-grants-1999_01
ORD IDord-b2fd024940104ae1a0b3ed8c078edffc
출처 메모uspto-grants-1999_01