HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 1-Methyl-5-thioureido-1H-imidazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-(3-Benzoyl-thioureido)-1-methyl-1H-imidazole-4-carboxylic acid amide | HCID 14897141 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Methyl-5-thioureido-1H-imidazole-4-carboxamide | HCID 14897145 | 96.9% |
Reaction Steps
5-(N'-benzoylthiocarbamoyl)amino-1-methyl-1H-imidazole-4-carboxamide (12.1 g, 40 mM) was added to a mixture of acetone and methanol (1:1) (200 ml). Potassium carbonate 2.8 g, 20 mM) dissolved in water (12 ml) was added. The reaction mixture was refluxed under N2 for 6 hours whereafter acetic acid (2.9 g, 48 mM) was added. After stirring in an ice bath the product was filtered off, washed and dried. Hereby was isolated 7.7 g (96%) of the title compound as a white powder, mp. 270°-274° C. (dec.) (the conversion begins at about 220° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05223619 |
| Source dataset | uspto-grants-1993_06 |
| ORD ID | ord-732d9a7c40c54724a344028f6849feab |
| Source note | uspto-grants-1993_06 |