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HRID 440914作成日:2026年10月25日

Dimethyl Sulfoxide → 2,4-Diamino-6-(2,3-dihydro-2,2-dimethyl-3-benzofuranon-7-yl)pteridine

https://huagongshe.com/reaction/440914

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物WaterHCID 962—
反応物TriethylamineHCID 8471—
反応物2,4-Diamino-6-(2,3-dihydro-3-hydroxy-2,2-dimethylbenzofuran-7-yl)pteridineHCID 19040781—
溶媒DichloromethaneHCID 6344—
生成物2,4-Diamino-6-(2,3-dihydro-2,2-dimethyl-3-benzofuranon-7-yl)pteridineHCID 86749513—

反応条件

温度-60 °C

反応手順

A stirring solution of 1.8 grams (0.011 mole) of pyridine-sulfur trioxide complex [prepared by the method of E. E. Gilbert, Chem. Rev., 62, 551-555 (1962)] in 25 mL of methylene chloride is cooled to -60° C., and a solution of 2.0 grams (0.024 mole) of dimethyl sulfoxide in 5 mL of methylene chloride is added dropwise during a 5 minute period. Upon completion of addition, the reaction mixture is stirred at -60° C. for about 10 minutes. After this time a solution of 3.2 grams (0.10 mole) of 2,4-diamino-6-(2,3-dihydro-3-hydroxy-2,2-dimethylbenzofuran-7-yl)pteridine in 10 mL of methylene chloride is added dropwise during a 5 minute period. Upon completion of addition, the reaction mixture is again stirred at -60° C. for about 10 minutes, and then 5.1 grams (0.050 mole) of triethylamine is added dropwise during a 5 minute period. The reaction mixture is then allowed to warm to ambient temperature. After this time 30 mL of water is added, and the mixture is stirred for about 10 minutes. The aqueous layer is separated and extracted with about 20 mL of methylene chloride. The extract is combined with the organic layer, and the combination is concentrated under reduced pressure, yielding 2,4-diamino-6-(2,3-dihydro-2,2-dimethyl-3-benzofuranon-7-yl)pteridine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05521190
出典データセットuspto-grants-1996_05
ORD IDord-8862b8d55c3c4ad6afab86d63ca74a1b
出典メモuspto-grants-1996_05