HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylethanimidothioate hydroiodide → HCID 178465574, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylethanimidothioate hydroiodide | HCID 11680130 | — |
| Reactant | N-(4-[2-(4-aminophenyl)ethyl]-5-[4-(methylsulfonyl)benzyl]-1,3-thiazol-2-yl)acetamide | HCID 21914845 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178465574 | HCID 178465574 | 46.7% |
Reaction Steps
N-{4-[2-(4-Aminophenyl)ethyl]-5-[4-(methylsulfonyl)benzyl]-1,3-thiazol-2-yl}acetamide (200 mg), methyl ethanimidothioate hydroiodide (202 mg) and MeOH (4 ml) were combined under N2 atmosphere. The reaction mixture was refluxed for 3 hours. After cooled to room temperature, the mixture was concentrated in vacuo. The residue was purified by preparative NH silica gel chromatography with CHCl3/MeOH (10:1) as an eluent. The amorphous substance was solidified with ethyl ether to give N-{4-{2-[4-(ethanimidoylamino)phenyl]ethyl}-5-[4-(methylsulfonyl)benzyl]-1,3-thiazol-2-yl}acetamide (102.4 mg) as a pale yellow amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07125901B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-c243f59e51b9466eb44a7b41959e5413 |
| Source note | uspto-grants-2006_10 |