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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530716Generated: November 3, 2026

1-Tert-butylpiperazine → HCID 68313151, compound

https://huagongshe.com/reaction/1530716

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Tert-butylpiperazineHCID 3530572—
ReactantHCID 86671484HCID 86671484—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 68313151HCID 68313151—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1-{4-[3-methyl-1-(propan-2-yl)-1H-1,2,4-triazol-5-yl]-9-oxa-3,6,12-triazatricyclo[8.4.0.02,6]tetradeca-1(14),2,4,10,12-pentaen-13-yl}ethyl methanesulfonate (240 mg) and 1-tert-butylpiperazine (281 mg, 1.97 mmol) in dioxane (5.00 mL) was stirred at 100° C. for 16 hrs under N2 atmosphere. After removal of the solvents, the residue was purified with reverse phase Combi-flash eluting with a 20-28% gradient of CH3CN in 0.3% NH4HCO3 to afford the desired product. The isolated solid was further separated by chiral SFC (AD-H column, EtOH (0.1% DEA) isocratic) to give the two enantiomers 303 and 305.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090628B2
Source datasetuspto-grants-2015_07
ORD IDord-7e86bbe5a0254675b5c4ba44f936c719
Source noteuspto-grants-2015_07