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HRID 1362933作成日:2026年10月25日

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

https://huagongshe.com/reaction/1362933

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Nicotinic acid, hydrazideHCID 11112—
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acidHCID 44630704—
溶媒DimethylformamideHCID 6228—
生成物Pyridine-3-carboxylic acid N'-(5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carbonyl)hydrazideHCID 59830438—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07884112B2
出典データセットuspto-grants-2011_02
ORD IDord-289e93d2f1644254a1d4659a32b7a4aa
出典メモuspto-grants-2011_02