HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201296Generated: October 29, 2026
4,4-Diethoxybutylamine → HCID 86723419, compound
https://huagongshe.com/reaction/2201296
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4,4-Diethoxybutylamine | HCID 80672 | — |
| Reactant | 5-Benzoyl-6-(bromomethyl)-1,3-dimethylpyrimidine-2,4(1H,3H)-dione | HCID 950319 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86723419 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359381B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-423e8c4b44fb404785e5d55b1f5fa0fa |
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| Source note | uspto-grants-2016_06 |
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