HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Toluenesulfonylhydrazide → 4-(4-Carboxyphenyl)-1-[2-methoxy-3-(4-methylphenyl)benzylidene]-3-thiosemicarbazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Toluenesulfonylhydrazide | HCID 15303 | — |
| Reactant | 4-(4-Carboxyphenyl)-3-thiosemicarbazide | HCID 2757378 | — |
| Reactant | 2-Methoxy-3-(4-methylphenyl)benzaldehyde | HCID 22566703 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-Carboxyphenyl)-1-[2-methoxy-3-(4-methylphenyl)benzylidene]-3-thiosemicarbazide | HCID 86591501 | 14.3% |
Reaction Steps
A solution of 4-(4-carboxyphenyl)-3-thiosemicarbazide (11 mg, 0.05 mmol) and 2-methoxy-3-(4-methylphenyl)benzaldehyde (14 mg, 0.06 mmol) in dimethylformamide (1 mL) was shaken with 4 Å molecular sieves for 40 h. PS-TsNHNH2 resin (17 mg, 0.05 mmol) was added and shaking continued for 24 h, then the resin was filtered off. The solvent was removed under vacuum and the residue chromatographed by reverse phase HPLC (CombiPrep ODS-A, 10–90% acetonitrile/water+0.1% trifluoroacetic acid) to give the title compound (3 mg, 14%) as a solid. MS (ES−) m/e 418 [M−H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07241783B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-fc0359c5821e46069c85985ba538fb6c |
| Source note | uspto-grants-2007_07 |