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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458637Generated: October 25, 2026

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

https://huagongshe.com/reaction/458637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantAzepan-3-amineHCID 2756445—
Reactant8-Bromo-7-(2-bromobenzyl)-3-methyl-3,7-dihydropurine-2,6-dioneHCID 22508575—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
Product8-(3-Aminoazepan-1-yl)-7-(2-bromobenzyl)-3-methyl-3,7-dihydropurine-2,6-dioneHCID 22508638—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192952B2
Source datasetuspto-grants-2007_03
ORD IDord-f63a5f954fff49b69eb65b75e3ab1433
Source noteuspto-grants-2007_03