HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N-[2-(4-Chloro-N-methylcinnamylamino)ethyl]-5-isoquinolinesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | N-[2-(4-Chlorocinnamylamino)ethyl]-5-isoquinolinesulfonamide | HCID 176156 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-[2-(4-Chloro-N-methylcinnamylamino)ethyl]-5-isoquinolinesulfonamide | HCID 53675817 | — |
Reaction Steps
1.50 g of the product of Example 172 was dissolved in 10 ml of chloroform, to the solution was added 3 ml of methyl iodide at a room temperature, and the mixture was stirred for 40 minutes. Excess methyl iodide was immediately evaporated off under a reduced pressure, and resulting residue was purified on a silica gel column (silica gel 50 g, eluant: 5% methanol in chloroform), to obtain 720 mg of the title compound in a colorless amorphous form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05081246 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-9a35a85cc674415a888b7e3a55a21420 |
| Source note | uspto-grants-1992_01 |