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HRID 405186作成日:2026年10月25日

Ethanol → Ethyl 3-(5-(2-(((4'-chloro-[1,1'-biphenyl]-4-yl)amino)methyl)-3,5-bis(trifluoromethyl)phenyl)picolinamido)propanoate

https://huagongshe.com/reaction/405186

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物4-Amino-4'-chlorodiphenylHCID 8675—
反応物Sodium borohydrideHCID 4311764—
反応物Ethyl 3-(5-(2-formyl-3,5-bis(trifluoromethyl)phenyl)picolinamido)propanoateHCID 86674260—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 3-(5-(2-(((4'-chloro-[1,1'-biphenyl]-4-yl)amino)methyl)-3,5-bis(trifluoromethyl)phenyl)picolinamido)propanoateHCID 86674261—

反応条件

温度100 °C

反応手順

Ethyl 3-(5-(2-formyl-3,5-bis(trifluoromethyl)phenyl)picolinamido)propanoate (76 mg, 0.16 mmol) and 4′-chloro-[1,1′-biphenyl]-4-amine (40 mg, 0.20 mmol) in DMSO (0.16 mL) was stirred at 100° C. After 30 min EtOH (0.16 mL) was added and the resulting homogeneous solution was stirred at 100° C. After 1 h the resulting homogeneous solution was cooled to room temperature, and NaBH4 (20 mg, 0.53 mmol), EtOH (1 mL), and DMSO (0.5 mL) were added and the resulting mixture was stirred. After 30 min, additional NaBH4 (20 mg, 0.53 mmol) was added and the resulting homogeneous solution was stirred. After 20 min the resulting mixture was diluted with DCM (5 mL) and 1 M NaH2PO4 (4 mL) was carefully added. Water was added and the aqueous phase was extracted with DCM. The combined organic layers were dried (Na2SO4), concentrated, and purified via column chromatography to yield the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08748624B2
出典データセットuspto-grants-2014_06
ORD IDord-cf1fef51d5b3431c96f6ea6a8cd4ae49
出典メモuspto-grants-2014_06