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HRID 458637作成日:2026年10月26日

Water → 8-(3-Aminoazepan-1-yl)-7-(2-bromobenzyl)-3-methyl-3,7-dihydropurine-2,6-dione

https://huagongshe.com/reaction/458637

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Azepan-3-amineHCID 2756445—
反応物8-Bromo-7-(2-bromobenzyl)-3-methyl-3,7-dihydropurine-2,6-dioneHCID 22508575—
溶媒Dimethyl SulfoxideHCID 679—
溶媒DichloromethaneHCID 6344—
生成物8-(3-Aminoazepan-1-yl)-7-(2-bromobenzyl)-3-methyl-3,7-dihydropurine-2,6-dioneHCID 22508638—

反応手順

8-Bromo-7-(2-bromobenzyl)-3-methyl-3,7-dihydropurine-2,6-dione (80A) (300 mg, 0,7 mmol) and azepan-3-ylamine (248 mg, 2,2 mmol), and triethylamine (0.5 ml, 3,6 mmol) were dissolved in 3 ml of DMSO and the mixture was subjected to microwaves (method F, 200° C., 300 W) for 30 minutes. To the reaction mixture was added 100 ml of water and 100 ml of dichloromethane, and the organic layer was separated and dried over sodium sulfate. The solvents were evaporated and the crude product was purified by preparative HPLC (method A1, Rt=7.17 min.). Evaporation of the solvent afforded the title compound as an brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07192952B2
出典データセットuspto-grants-2007_03
ORD IDord-f63a5f954fff49b69eb65b75e3ab1433
出典メモuspto-grants-2007_03