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HRID 8739作成日:2026年10月23日

Bromobenzene → Ammonium Hydroxide

https://huagongshe.com/ja/reaction/8739

反応式

関与物質

役割名称HCID仕込み量
反応物BromobenzeneHCID 7961—
反応物Potassium CarbonateHCID 11430—
反応物TriphenylphosphineHCID 11776—
反応物5,6,7,8-Tetrahydroimidazo(1,2-a)pyrazineHCID 13247046—
反応物2-Chloro-6,7-dimethoxy-3H-quinazolin-4-oneHCID 135456664—
反応物HCID 178419040HCID 178419040—
触媒palladium(II) acetateHCID 167845—
溶媒DimethylformamideHCID 6228—
生成物Ammonium HydroxideHCID 14923—
生成物HCID 178418711HCID 178418711—

反応条件

温度140 °C

反応手順

5,6,7,8-Tetrahydro-imidazo[1,2-a]pyrazine, prepared as described in PCT Application WO 01/44250, was coupled with 2-chloro-6,7-dimethoxy-3H-quinazolin-4-one 1b, as described herein. 2-(5,6-dihydro-8H-imidazo[1,2-a]pyrazin-7-yl)-6,7-dimethoxy-1H-quinazolin-4-one (150 mg, 0.46 mmol) was combined with bromobezene (97 μL, 0.92 mmol), potassium carbonate (127 mg, 0.92 mmol), palladium acetate (5 mg, 5 mol %), and triphenylphosphine (13 mg, 10 mol %) in DMF (6 mL). The mixture was heated in a 140° C. bath for 2 d, then concentrated onto silica gel followed by eluting with 300:10:1 CH2Cl2:MeOH:NH4OH) to afford 50 mg of 6,7-dimethoxy-2-(3-phenyl-5,6-dihydro-8H-imidazo[1,2-α]pyrazin-7-yl)-1H-quinazolin-4-one, 904, mp: >300° C, M+=403.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091200B2
出典データセットuspto-grants-2006_08
ORD IDord-6647c4f09b6c419a9d4dc6d55a619a4e
出典メモuspto-grants-2006_08