Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | HCID 11680688 | HCID 11680688 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11565825 | HCID 11565825 | 44% |
Reaction Steps
To a solution of 1-[(1E)-1-buten-3-ynylsulfonyl]-4-(2-pyridinyl)piperazine (30 mg; 0.11 mmol; 1.00 eq.) in THF (3 mL) was added an aq. solution of hydroxylamine (50%, 0.10 mL; 1.62 mmol; 15.0 eq.) and the resulting reaction mixture was stirred at 60° C. for 4 h. Evaporation of the solvents (rotavap gave an oil). Purification on silicagel (50/50 up to 70/30 AcOEt-c-Hex) a colorless oil (15 mg, 44% yield). LC/MS, M+ (ESI): 311.1, M−(ESI): 311.1, M− (ESI): 309.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07973039B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-2c08ffcef1694e71bf83d25f2b4ccb3b |
|---|
| Source note | uspto-grants-2011_07 |
|---|