Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cinnamoylbenzene | HCID 7189 | — |
| Reactant | Benzenesulfonyl hydrazide | HCID 65723 | — |
| Product | HCID 22251491 | HCID 22251491 | 31% |
Reaction Steps
To a stirred solution at room temperature of chalcone XXIIIa (1.29 g, 5.13 mmol) in DMF (20 ml) was added phenylsulfonylhydrazine (1.76 g, 10.26 mmol). The reaction mixture was stirred at 10° C. for 15 h, cooled and concentrated. The remained oily residue was partitioned between a saturated aqueous solution of NH4Cl and AcOEt. After separation, the organic layer was dried, partially evaporated and filtered. The filtrate was purified by flash chromatography on silica gel (AcOEt/hexane:50/50□75/25) to form a material which after a second column purification (MeOH/CH2Cl2:5/95) afford the title compound XXVIa (400 mg, 1.59 mmol, 31% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07282608B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-4e3bb493536b462bbd8696117c8e9a66 |
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| Source note | uspto-grants-2007_10 |
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