HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 4-chloro-3-methoxy-10-methyl-10H-phenothiazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-chloro-3-hydroxy-10H-phenothiazine | HCID 9881418 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-chloro-3-methoxy-10-methyl-10H-phenothiazine | HCID 13882027 | — |
Reaction Steps
To 25 ml of DMF was added methyl iodide (2.9 ml), 4-chloro-3-hydroxy-10H-phenothiazine (see Example 3) (2.3 g) and sodium hydride (0.672 g). The resulting reaction mixture was stirred at ambient temperature for 12 hours. At 0° C., MeOH was added to destroy the remaining hydride, then H2O. The resulting solution was extracted with ethyl acetate and the organic phase, dried and evaporated. The resulting residue was then purified by chromatography on silica gel to give 1.5 g of 4-chloro-3-methoxy-10-methyl-10H-phenothiazine (m.p.: 136° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04845083 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-3ca45229dee74b15b5ff8be4ddb772df |
| Source note | uspto-grants-1989_07 |