HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530716Generated: November 3, 2026
1-Tert-butylpiperazine → HCID 68313151, compound
https://huagongshe.com/reaction/1530716
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Tert-butylpiperazine | HCID 3530572 | — |
| Reactant | HCID 86671484 | HCID 86671484 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 68313151 | HCID 68313151 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090628B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-7e86bbe5a0254675b5c4ba44f936c719 |
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| Source note | uspto-grants-2015_07 |
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