戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 303作成日:2026年10月24日

2-(Trifluoromethyl)benzylamine → 6-[[2-(Trifluoromethyl)phenyl]methylamino]pyridine-3-carboxamide

https://huagongshe.com/ja/reaction/303

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Trifluoromethyl)benzylamineHCID 76447—
反応物6-ChloronicotinamideHCID 80456—
試薬Sodium t-butoxideHCID 23676156—
触媒Binap, (A+-)-HCID 634876—
触媒Palladium (II) acetateHCID 4144353—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物6-[[2-(Trifluoromethyl)phenyl]methylamino]pyridine-3-carboxamideHCID 789827341.45%

反応条件

温度120 °C

反応手順

To a stirred solution of 6-chloronicotinamide (0.053 g, 0.34 mmol), 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (0.021 g, 0.03 mmol), sodium 2-methylpropan-2-olate (0.065 g, 0.68 mmol) and diacetoxypalladium (7.60 mg, 0.03 mmol) in DME (1 mL) was added (2-(trifluoromethyl)phenyl)methanamine (0.095 mL, 0.68 mmol). The reaction mixture was subjected to microwave irradiation for 4h at 120 C. Only traces of product was observed. The crude product was dissolved in DMSO (2 mL) and purified using Fractionlynx I, (Xbridge Prep C18 5µm OBD 19x150 mm column), with 5 to 95% acetonitrile in 0.2% ammonia at pH 10. 6-(2-(trifluoromethyl)benzylamino)nicotinamide: 1.45 mg (1.5 %)

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-c7ac817750064edba47d3c6c786a7b69
出典メモ750 AstraZeneca ELN dataset