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HRID 2194403作成日:2026年10月26日

Water → 6-[4-(3-chloro-phenylethynyl)-2-methyl-imidazol-1-yl]-1H-pyrazin-2-one

https://huagongshe.com/reaction/2194403

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物PhenylsilaneHCID 12752—
反応物2-Allyloxy-6-[4-(3-chloro-phenylethynyl)-2-methyl-imidazol-1-yl]-pyrazineHCID 66865611—
溶媒DichloromethaneHCID 6344—
生成物6-[4-(3-chloro-phenylethynyl)-2-methyl-imidazol-1-yl]-1H-pyrazin-2-oneHCID 6686536645.3%

反応手順

A solution of 75 mg (0.214 mmol) 2-Allyloxy-6-[4-(3-chloro-phenylethynyl)-2-methyl imidazol-1-yl]-pyrazine in 5 ml of methylene chloride was degassed with argon. Then 0.052 ml (0.428 mmol) of phenyl silane and 2.5 mg (0.002 mmol) of tetrakis(triphenyl-phosphine)palladium were added and the mixture was stirred for 1 h at room temperature. Then water (1 ml) was added and the mixture was vigourously stirred for 5 min., diluted with 10 ml of methylene chloride and the organic phase was washed with water and brine, dried over magnesium sulfate and concentrated. The obtained solid was triturated with benzene to remove impurities (triphenylphosphine oxide), filtered and dried to yield 30 mg (0.097 mmol, 45%) of the title compound as a white crystalline solid, MS: m/e=311.1, 313.1 (M+H+)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08334287B2
出典データセットuspto-grants-2012_12
ORD IDord-3d334f4b4c1f4ce09d63fa3ca7a79fdd
出典メモuspto-grants-2012_12