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HRID 2092540作成日:2026年10月27日

Dimethylformamide → 4-(2-Chloro-7-(3-(methylsulfonyl)phenyl)quinazolin-4-yl)morpholine

https://huagongshe.com/reaction/2092540

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Sodium CarbonateHCID 10340—
反応物3-(Methylsulfonyl)phenylboronic acidHCID 2773542—
反応物4-(7-Bromo-2-chloroquinazolin-4-yl)morpholineHCID 86665758—
触媒HCID 178418476HCID 178418476—
溶媒WaterHCID 962—
生成物4-(2-Chloro-7-(3-(methylsulfonyl)phenyl)quinazolin-4-yl)morpholineHCID 8666576080%

反応条件

温度95 °C

反応手順

To a 50 mL round bottom flask, 7-bromo-2-chloro-4-morpholin-4-yl-quinazoline (0.65 g, 0.0019 mol), 3-methylsulfonylphenylboronic acid (0.35 g, 0.0018 mol), sodium carbonate (0.314 g, 0.0029 mol), DMF (25 mL) and water (6 mL) were added and degassed the reaction vessel with nitrogen for 5-10 min. To the same reaction mixture, Pd(PPh3)2Cl2 (0.069 g, 0.00099 mol) was added and again degassed with nitrogen for 5-10 min. The reaction mixture was stirred at 95° C. for 2 h. The reaction mixture was cooled and diluted with ethyl acetate. The organic layer was washed with water, brine and dried over sodium sulfate. The solvent was removed under reduced pressure to afford the crude product. The crude product was purified; using column chromatography (60-120 silica gel, 50% ethyl acetate in hexane) to yield the desired product [400 mg, 80%]. LC-MS (ESI): Calculated mass: 403.1; Observed mass: 404.0 [M+H]+ (RT: 1.36 min).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08440662B2
出典データセットuspto-grants-2013_05
ORD IDord-e4dfa962c1164b40a076c49ed9b656c8
出典メモuspto-grants-2013_05