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HRID 2217997作成日:2026年10月25日

Dimethylformamide → 3-(8-Methoxy-1-methyl-2-oxo-7-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-5-yl)-benzonitrile

https://huagongshe.com/reaction/2217997

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物Phenylboronic AcidHCID 66827—
反応物3-(7-bromo-8-methoxy-1-methyl-2-oxo-2,3-dihydro-1H-benzo[e][1,4]diazepin-5-yl)-benzonitrileHCID 69287738—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
生成物3-(8-Methoxy-1-methyl-2-oxo-7-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-5-yl)-benzonitrileHCID 1124600860%

反応条件

温度120 °C

反応手順

To 5 mL of degazed DMF were added 3-(7-bromo-8-methoxy-1-methyl-2-oxo-2,3-dihydro-1H-benzo[e][1,4]diazepin-5-yl)-benzonitrile Intermediate 9 (200 mg, 0.52 mmol), benzene boronic acid (160 mg, 1.32 mmoles), tripotassium phosphate (300 mg, 1.42 mmol), Pd(PPh3)4 (30 mg, 0.03 mmoles). The mixture was stirred for 16 hours at 120° C. under nitrogen atmosphere. The working solution was diluted ten times with water and extracted three times with ethyl acetate. The organic phase was dried over Na2SO4 and concentrated until dryness. The residue was chromatographied: eluant: CH2Cl2/Et2O: 1/1. The obtained compound was crystallised from ether/pentane to afford the title compound (118 mg): white solid, (yield=60%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07410963B2
出典データセットuspto-grants-2008_08
ORD IDord-4e8c41ee64c2471caf0dee8a161db175
出典メモuspto-grants-2008_08