HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2-(methylthio)-7-chloro-5-phenyl-3H-1,5-benzodiazepin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 7-chloro-5-phenyl-1H-1,5-benzodiazepin-4-one-2-thione | HCID 12264319 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(methylthio)-7-chloro-5-phenyl-3H-1,5-benzodiazepin-4-one | HCID 20329323 | — |
Reaction Steps
To 3.03 g of 7-chloro-5-phenyl-1H-1,5-benzodiazepin-4-one-2-thione in a solution of 0.40 g sodium hydroxide and 15 ml of methanol is added, with stirring a solution of 1.39 g of methyl iodide in 5 ml of methanol. Stirring is continued for 1 hour, the reaction is evaporated, diluted with 30 ml methylene chloride and filtered through a short Florisil column. After washing the column with ethyl acetate, the combined filtrates are evaporated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04213982 |
| Source dataset | uspto-grants-1980_07 |
| ORD ID | ord-138800247c4c434aaf8ac87458a4a02f |
| Source note | uspto-grants-1980_07 |