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HRID 346680作成日:2026年10月27日

Triethylamine → 1-(4-Pyridyl)-(5-(6-methoxyindol-2-ylcarbonylamino)pyrid-2-yloxy)pyrrolidine

https://huagongshe.com/reaction/346680

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物5-Methoxyindole-2-carboxylic acidHCID 20401—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物Sodium BicarbonateHCID 516892—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物1-(4-Pyridyl)-3-(5-amino-2-pyridyloxy)pyrrolidineHCID 17915767—
溶媒DimethylformamideHCID 6228—
生成物1-(4-Pyridyl)-(5-(6-methoxyindol-2-ylcarbonylamino)pyrid-2-yloxy)pyrrolidineHCID 17915739—

反応手順

To a solution of 5-methoxyindole-2-carboxylic acid (168 mg, 0.88 mmol) in DMF (4 ml) was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (168 mg, 0.88 mmol), 1-hydroxybenzotriazole (118 mg, 0.88 mmol) and Et3N (0.12 ml, 0.88 mmol) followed by 1-(4-pyridyl)-3-(5-amino-2-pyridyloxy)pyrrolidine (150 mg, 0.58 mmol) and the resulting suspension stirred at room temperature for 7 days. The mixture was poured into saturated aqueous NaHCO3 solution and the solid precipitate collected by filtration and washed with water then dried (over P2O5) to give 1-(4-pyridyl)-(5-(6-methoxyindol-2-ylcarbonylamino)pyrid-2-yloxy)pyrrolidine as an off white solid (195 mg);

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07173025B1
出典データセットuspto-grants-2007_02
ORD IDord-f371cd3f91514211a46171d1ef93ed8a
出典メモuspto-grants-2007_02