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HRID 2201152作成日:2026年10月24日

Water → 1-(6-Chloro-5-cyano-3-fluoropyridin-2-ylamino)cyclopentanecarboxamide

https://huagongshe.com/ja/reaction/2201152

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物DiisopropylethylamineHCID 81531—
反応物2,6-Dichloro-5-fluoro-3-pyridinecarbonitrileHCID 2733849—
反応物1-Aminocyclopentane-1-carboxamide hydrochlorideHCID 54593188—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Ethyl AcetateHCID 8857—
生成物1-(6-Chloro-5-cyano-3-fluoropyridin-2-ylamino)cyclopentanecarboxamideHCID 8666616749%

反応手順

A solution of 2,6-dichloro-3-cyano-5-fluoropyridine (250 mg, 1.30 mmol), 1-aminocyclopentanecarboxamide hydrochloride (214 mg, 1.30 mmol) and DIEA (0.650 mL, 3.73 mmol) in DMSO (3 mL) was stirred at 95 C for 4 h. Water and EtOAc were added. The organic phase was separated, dried over Na2SO4, concentrated in vacuo. The residue was purified by a silica gel column, eluted with 50-100% EtOAc in hexane to give 1-(6-chloro-5-cyano-3-fluoropyridin-2-ylamino)cyclopentanecarboxamide (180 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09359375B2
出典データセットuspto-grants-2016_06
ORD IDord-9b1b06fdd12d443bb23d15c821cf8101
出典メモuspto-grants-2016_06