HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 20268267, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 13371473 | HCID 13371473 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20268267 | HCID 20268267 | — |
Reaction Steps
[II; R=5-CH3O, R'=CH3, R"=H, OR°=4-OCH2C6H5, Alk=CH3 ] is obtainable by N-alkylation of 1-[2-(4-benzyloxyphenylamino)-5-methoxyphenyl]ethanone (Example 1b) with methyl iodide in the presence of sodium hydride. A preferred procedure is to add slowly methyl iodide in excess to a cooled (0° C.) suspension of starting material and sodium hydride in an inert solvent, e.g. dimethylformamide, and stirring the reaction mixture at ambient temperature until the reaction is complete.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04539429 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-a7688f66d4c1468faf46248f286a03ac |
| Source note | uspto-grants-1985_09 |