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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829669Generated: October 31, 2026

1,4-Dioxane → HCID 22053578, compound

https://huagongshe.com/reaction/1829669

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-AcetylpiperazineHCID 83795—
Reactant6-[3,5-Bis(trifluoromethyl)benzyl]-5,6,7,8,9,10-hexahydro-4-(2-methylphenyl)-2-(methylsulfonyl)-5-oxopyrimido[4,5-b][1,5]diazocineHCID 22053591—
ProductHCID 22053578HCID 2205357891%

Reaction Conditions

Temperature100 °C

Reaction Steps

1-acetylpiperazine (23.1 mg), diisopropylethylamine (0.1 mL), and 1,4-dioxane (1 mL) were added to 6-[3,5-bis(trifluoromethyl)benzyl]-5,6,7,8,9,10-hexahydro-4-(2-methylphenyl)-2-(methylsulfonyl)-5-oxopyrimido[4,5-b][1,5]diazocine (Compound of Reference Example 19; 85.9 mg). While heated, the mixture was refluxed for 5 hours. The solvent was removed and anhydrous acetic acid (0.5 mL) and pyridine (0.1 mL) were added, followed by stirring at 100° C. for 3 hours. Subsequently, the reaction mixture was diluted with ethyl acetate, was sequentially washed with water and a saturated aqueous solution of sodium chloride, and was then dried over anhydrous sodium sulfate. Following removal of the solvent, the residue was purified on a silica gel column chromatography (ethyl acetate:methanol=10:1) to obtain 10-acetyl-2-(4-acetylpiperazine-1-yl)-6-[3,5-bis(trifluoromethyl)benzyl]-5,6,7,8,9,10-hexahydro-4-(2-methylphenyl)-5-oxopyrimido[4,5-b][1,5]diazocine (90.2 mg, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064119B2
Source datasetuspto-grants-2006_06
ORD IDord-637c6e824d044429badc18dee0ece630
Source noteuspto-grants-2006_06