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HRID 2116574作成日:2026年10月25日

Benzylacetylene → 2-(Methylthio)-6-benzyl-furano[2,3-d]pyrimidine

https://huagongshe.com/reaction/2116574

反応式

関与物質

役割名称HCID仕込み量
反応物BenzylacetyleneHCID 575753—
反応物HCID 178418710HCID 178418710—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
溶媒TriethylamineHCID 8471—
溶媒Ethyl AcetateHCID 8857—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物2-(Methylthio)-6-benzyl-furano[2,3-d]pyrimidineHCID 21039980—

反応条件

温度40 °C

反応手順

A mixture of 2-methylthio-4-hydroxy-5-iodopyrimidine (2.65 g), 3-phenyl-1-propyne (1.49 mL), copper (I) iodide (90 mg) and bis(triphenylphosphine) Palladium (II) dichloride (Fluka, 160 mg) in 20 mL of triethylamine and NMP (7 mL) was stirred at 40° C. for 6 hours. The reaction mixture was diluted with ethyl acetate (100 mL), washed with brine (3×50 mL), concentrated and purified by column chromatography (5% EtOAc/hexanes) to give 0.57 g of a solid product. MP: 69-72.2° C. MS: 257.2 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07439247B2
出典データセットuspto-grants-2008_10
ORD IDord-661b12ef911749cfb66470dac867c9d2
出典メモuspto-grants-2008_10