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HRID 963391作成日:2026年10月25日

Water → 5-[3-Trimethylsilyl-ethynyl-4,5-dimethoxy-benzyl]-pyrimidine-2,4-diamine

https://huagongshe.com/reaction/963391

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriethylamineHCID 8471—
反応物TrimethylsilylacetyleneHCID 66111—
反応物5-(3,4-Dimethoxy-5-iodo-benzyl)pyrimidine-2,4-diamineHCID 11101094—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒DimethylformamideHCID 6228—
生成物5-[3-Trimethylsilyl-ethynyl-4,5-dimethoxy-benzyl]-pyrimidine-2,4-diamineHCID 1908154459%

反応手順

A mixture of 8.7 g of 5-(3,4-dimethoxy-5-iodobenzyl)-pyrimidine-2,4-diamine, 6.2 ml of ethynyltrimethylsilane, 80 mg of bis-trimethylphosphine-palladium dichloride and 1 mg of copper(I) iodide in 25 ml of triethylamine and 25 ml of dimethylformamide is stirred at 60° for 16 hrs. After cooling to room temperature the reaction mixture is treated with 400 ml of water and extracted three times with 200 ml of methylene chloride each time. The combined organic phases are washed twice with 250 ml of water, once with 250 ml of a saturated sodium chloride solution and dried over magnesium sulphate. The crude product is chromatographed on silica gel with methylene chloride/methanol 9:1. 4.73 g (59%) of 5-[3-trimethylsilyl-ethynyl-4,5-dimethoxy-benzyl]-pyrimidine-2,4-diamine are obtained as beige crystals. M.p. 189°-190°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05763450
出典データセットuspto-grants-1998_06
ORD IDord-796060440b9c4307b5154120d4c9930d
出典メモuspto-grants-1998_06