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HRID 2251992作成日:2026年10月25日

(2-Bromopyridin-3-yl)-(2-chlorophenyl)methanone → {2-[1-(3,5-bis-trifluoromethyl-benzyl)-5-methyl-1H-[1,2,3]triazol-4-yl]-pyridin-3-yl}-(2-chloro-phenyl)-methanone

https://huagongshe.com/reaction/2251992

反応式

関与物質

役割名称HCID仕込み量
反応物(2-Bromopyridin-3-yl)-(2-chlorophenyl)methanoneHCID 85882881—
反応物1-(3,5-bis-trifluoromethyl-benzyl)-5-methyl-4-tributylstannanyl-1H-[1,2,3]triazoleHCID 86601250—
溶媒DimethylformamideHCID 6228—
生成物{2-[1-(3,5-bis-trifluoromethyl-benzyl)-5-methyl-1H-[1,2,3]triazol-4-yl]-pyridin-3-yl}-(2-chloro-phenyl)-methanoneHCID 5964454354.1%

反応条件

温度80 °C

反応手順

Dissolve (2-bromo-pyridin-3-yl)-(2-chloro-phenyl)-methanone (148 mg, 0.50 mmol) and 1-(3,5-bis-trifluoromethyl-benzyl)-5-methyl-4-tributylstannanyl-1H-[1,2,3]triazole (449 mg, 0.75 mmol) in DMF (5 mL) and degass, then add dichlorobis(triphenylphosphine) palladium (70 mg, 0.10 mmol). Seal the mixture under N2 and heat at 80° C. for 24 hours. Concentrate, dissolve in CHCl3, wash with saturated potassium fluoride solution (2×), saturated potassium bicarbonate solution, brine, dry over MgSO4 and concentrate. Purify the residue by flash chromatography on silica gel eluting with 0-40% EtOAc/hexane followed by recrystallization from EtOAc/hexane to afford the title compound (142 mg, 54%). MS(IS) 525 (M+1); TLC (60% EtOAc/hexane) Rf=0.30.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07320994B2
出典データセットuspto-grants-2008_01
ORD IDord-5336a7072567493f9c1fd83e095dbb6a
出典メモuspto-grants-2008_01