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HRID 2201288作成日:2026年10月27日

Water → 3-(1,3-Dimethyl-2,4-dioxo-6-(2-(tritylthio)ethyl)-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-5-yl)benzonitrile

https://huagongshe.com/reaction/2201288

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物3-BromobenzonitrileHCID 23381—
反応物Barium hydroxideHCID 6093286—
反応物1,3-Dimethyl-2,4-dioxo-6-(2-(tritylthio)ethyl)-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-5-ylboronic acidHCID 86723522—
溶媒DichloromethaneHCID 6344—
溶媒Butyl AcetateHCID 31272—
生成物3-(1,3-Dimethyl-2,4-dioxo-6-(2-(tritylthio)ethyl)-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-5-yl)benzonitrileHCID 86723523—

反応条件

温度80 °C

反応手順

A suspension comprising 1,3-dimethyl-2,4-dioxo-6-(2-(tritylthio)ethyl)-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-5-ylboronic acid (Intermediate F) (300 mg, 0.571 mmol), 3-bromobenzonitrile (104 mg, 0.571 mmol) and barium hydroxide (196 mg, 1.142 mmol) in n-BuOAc (5710 μL) was treated with Pd-118 (18.61 mg, 0.029 mmol) and the mixture was heated to 80° C. Water (247 μL, 13.70 mmol) was added at 80° C. and the suspension was stirred rapidly for 90 minutes. After cooling to RT, the mixture was allowed to stand at RT overnight. The mixture was diluted with DCM (50 ml) and washed with water (50 ml). The layers were separated and the aqueous portion was extracted with DCM (3×30 ml). The organics were combined and dried over MgSO4, filtered and concentrated. Purification of the crude product by trituration with EtOAc/iso-hexane afforded the title compound;

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09359381B2
出典データセットuspto-grants-2016_06
ORD IDord-4850ca5bab394087b91fa98af5f92589
出典メモuspto-grants-2016_06