HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 1-[2-(N-formyl-N-hydroxyamino)-2-phenylethanesulfonyl]-4-(4-fluorophenyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1-[2-(Hydroxyamino)-2-phenylethanesulfonyl]-4-(4-fluorophenyl)piperazine | HCID 11176421 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[2-(N-formyl-N-hydroxyamino)-2-phenylethanesulfonyl]-4-(4-fluorophenyl)piperazine | HCID 9931221 | 61% |
Reaction Steps
To a solution of 1-[2-(hydroxyamino)-2-phenylethanesulfonyl]-4-(4-fluorophenyl)piperazine (338 mg, 0.89 mmol) in THF (5 ml) and formic acid (2 ml) was added a preformed mixture of formic acid (2 ml) and acetic anhydride (0.5 ml). The mixture was stirred at room temperature for one hour. The mixture was evaporated in vacuo and toluene (2×5 ml) was added and evaporated in vacuo. The residue was taken in CH2Cl2-methanol (6 ml, 9:1) and silica (1 g) was added. The mixture was stirred for 18 hours. The silica was filtered off and rinsed with CH2Cl2-methanol (9:1). The residue was purified on silica gel (eluant: CH2Cl2-MeOH 4%) to give the title compound as a light orange solid (220 mg, 61%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07342020B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-da105836e9684960a6f252c9c79e7d30 |
| Source note | uspto-grants-2008_03 |