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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793338Generated: November 3, 2026

HCID 69256685, compound → HCID 69256990, compound

https://huagongshe.com/reaction/1793338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69256685HCID 69256685—
ReactantHCID 131725870HCID 131725870—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 69256990HCID 6925699016.1%

Reaction Steps

A mixture of intermediate (54) (0.058 mol) in dioxane (400 ml) was stirred. A mixture of intermediate (3) (0.029 mol) and CaO (2.4 g) was added. The reaction mixture was stirred at 140° C. for 16 hours. The solvent was evaporated. DCM and water was added to the residue. The separated organic layer was dried, filtered and the solvent was evaporated. The residue was purified by high-performance liquid chromatography over silica gel (eluent:CH2Cl2/(CH3OH/NH3) 90/10). The product fractions were collected and the solvent was evaporated. The residue was dissolved in ethanol and converted into the ethanedioic acid salt (1:1). The formed precipitate was filtered off and dried, yielding 1.5 g of (S)-1-[3-[[(2,3-dihydro[1,4]dioxino[2,3-b]pyridin-3-yl)methyl]amino]propyl]dihydro-2,4(1H,3H)-pyrimidinedione (compound 25), mp.186; [α]D20 =−37.46°, (c=26.56 mg/5 ml DMF).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07081453B2
Source datasetuspto-grants-2006_07
ORD IDord-c60ac8e4ac2c4b1f93c294d3f5c814f1
Source noteuspto-grants-2006_07