Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | HCID 18919292 | HCID 18919292 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18918843 | HCID 18918843 | 7% |
Reaction Steps
A solution of methylhydrazine (472 mg) and ethyl 1-[4-(4-chlorobenzoyl)benzyl]-5-formylimidazole-4-carboxylate (1.03 g) in ethanol (20 ml) was refluxed for 3 hours. After cooling to room temperature, concentrated sulfuric acid (0.2 ml) was added and the mixture was further refluxed for 21 hours. This reaction mixture was diluted with water and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (developer; chloroform:methanol=19:1) to provide the title compound as white powder (66 mg, yield 7%). 1H-NMR (CDCl3) δ: 3.90(3H,s), 5.47(2H,s), 7.31(2H,d,J=8.4Hz), 7.48(2H,d,J=8.4Hz), 7.73(2H,d,J=8.4Hz), 7.81(2H,d,J=8.4Hz), 7.92(1H,s), 8.00(1H,s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05753664 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-c36c82000af045a08b0bc62f658b16c6 |
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| Source note | uspto-grants-1998_05 |
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