HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylethanimidothioate hydroiodide → HCID 178465573, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylethanimidothioate hydroiodide | HCID 11680130 | — |
| Reactant | N-{4-[2-(4-aminophenyl)ethyl]thiazol-2-yl}acetamide | HCID 21914814 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178465573 | HCID 178465573 | 142.6% |
Reaction Steps
N-(4-(2-(4-Aminophenyl)ethyl)-1,3-thiazol-2-yl)acetamide (100 mg) prepared in a similar manner according to Step 6 of Production Example 1, methyl ethanimidothioate hydriodide (166 mg) and methanol (3 ml) were combined, and refluxed for 1.5 hours. After cooled to room temperature, the mixture was concentrated in vacuo. The residue was purified by flash column chromatography over NH silica gel with chloroform/methanol (20:1→10:1) as an eluent to give N-(4-{2-[4-(ethanimidoylamino)phenyl]ethyl}-1,3-thiazol-2-yl)acetamide (165 mg) as a pale yellow amorphous substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07442715B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-84a707cce56446ef8f40fc6a4009eccf |
| Source note | uspto-grants-2008_10 |