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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1362933생성일: 2026년 10월 25일

Triethylamine → Pyridine-3-carboxylic acid N'-(5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carbonyl)hydrazide

https://huagongshe.com/reaction/1362933

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Nicotinic acid, hydrazideHCID 11112—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acidHCID 44630704—
용매DimethylformamideHCID 6228—
생성물Pyridine-3-carboxylic acid N'-(5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carbonyl)hydrazideHCID 59830438—

반응 단계

To a solution of nicotinic acid hydrazide (35 mg, 0.25 mmol) in DMF (5 mL) was added triethylamine (88 μL, 0.64 mmol), 5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid (Preparation 8, 50 mg, 0.25 mmol), HOBt (34 mg, 0.25 mmol) and EDCI (50 mg, 0.28 mmol). The mixture was allowed to stir at rt for 16 h. The solvent was removed in vacuo and the residue was partitioned between water (100 mL) and ethyl acetate (100 mL). The organic layer was dried (MgSO4) and concentrated in vacuo to give an oil, which was purified by flash chromatography on silica gel (dichloromethane/methanol, 9/1) to give the title compound. m/z (ES+)=316 [M+H]+; RT=2.62 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07884112B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-289e93d2f1644254a1d4659a32b7a4aa
출처 메모uspto-grants-2011_02