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HRID 57395作成日:2026年10月26日

Potassium Phosphate, Tribasic → 1-(5-(3-(Trifluoromethyl)phenyl)pyrimidin-2-yl)ethanone

https://huagongshe.com/reaction/57395

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Phosphate, TribasicHCID 62657—
反応物2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
反応物3-(Trifluoromethyl)phenylboronic acidHCID 2734388—
反応物1-(5-Bromopyrimidin-2-yl)ethan-1-oneHCID 53488064—
触媒palladium(II) acetateHCID 167845—
溶媒TolueneHCID 1140—
生成物1-(5-(3-(Trifluoromethyl)phenyl)pyrimidin-2-yl)ethanoneHCID 8673017265.5%

反応手順

A cloudy solution of 1-(5-bromopyrimidin-2-yl)ethanone (300 mg, 1.49 mmol), 3-(trifluoromethyl)phenylboronic acid (567 mg, 2.98 mmol), K3PO4 (950 mg, 4.48 mmol), DavePhos ligand [2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl](59 mg, 0.15 mmol), and Pd(OAc)2 (17 mg, 0.075 mmol) in 6 mL toluene was heated at 100° C. for 1 h. The mixture was cooled to room temperature, and filtered through Celite. Filter cake was rinsed with 30 mL EtOAc. The filtrate was poured into 20 mL water. Layers were separated, and the aqueous was further extracted with EtOAc (20 mL). Combined organics were washed with water (20 mL) and brine (20 mL), dried over Na2SO4, filtered and concentrated directly onto silica gel. Column chromatography (10-100% EtOAc/heptane) gave 0.26 g 1-(5-(3-(trifluoromethyl)phenyl)pyrimidin-2-yl)ethanone as tan solid. MS m/z 267.1 (M+H)+. 1H NMR (400 MHz, CDCl3) δ 9.16 (s, 2H), 7.93-7.69 (m, 4H), 2.87 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434719B2
出典データセットuspto-grants-2016_09
ORD IDord-1308a2f6995e48148fcbb0c8db6844bd
出典メモuspto-grants-2016_09