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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201296Generated: October 29, 2026

4,4-Diethoxybutylamine → HCID 86723419, compound

https://huagongshe.com/reaction/2201296

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4-DiethoxybutylamineHCID 80672—
Reactant5-Benzoyl-6-(bromomethyl)-1,3-dimethylpyrimidine-2,4(1H,3H)-dioneHCID 950319—
SolventEthanolHCID 702—
ProductHCID 86723419HCID 86723419—

Reaction Steps

5-Benzoyl-6-(bromomethyl)-1,3-dimethylpyrimidine-2,4(1H,3H)-dione (Intermediate C), (1.169 g, 3.47 mmol) in EtOH (20 mL) was treated with 4,4-diethoxybutan-1-amine (0.659 mL, 3.81 mmol) and TEA (0.966 mL, 6.93 mmol) and the mixture heated at reflux for 50 min. The reaction mixture was cooled to RT and evaporated under reduced pressure. The residue was re-dissolved in THF (20 mL), 1M hydrochloric acid (3.47 mL) was added and the mixture stirred at RT for 1.5 h. The reaction mixture was diluted with EtOAc, washed with water, brine and the organic phase was dried over sodium sulphate and evaporated under reduced pressure. The residue was triturated with DCM/hexane and the precipitate collected by filtration to give the title product as a pale pink solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359381B2
Source datasetuspto-grants-2016_06
ORD IDord-423e8c4b44fb404785e5d55b1f5fa0fa
Source noteuspto-grants-2016_06