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 of sodium hydroxide and 15 ml of methanol is added, with stirring a solution of 1.4 g of methyl iodide in 10 ml of methanol. Stirring is continued for 1 hour, the reaction is then evaporated and suspended in methylene chloride (30 ml). The suspension is filtered through a short Florisil column; the column is washed with ethyl acetate and the combined filtrates are evaporated. The residue is triturated with a minimum amount of absolute ethanol and the title compound is filtered off and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04070355 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-1f7f0f4a31b24cb3b98faf2336c3e880 |
| Source note | uspto-grants-1978_01 |