HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 7-Chloro-4-methyl-10-(methylthio)-4H-thieno[3,4-b][1,5]benzodiazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Methyl sulfate(1-) | HCID 4694097 | — |
| Reactant | HCID 12521656 | HCID 12521656 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7-Chloro-4-methyl-10-(methylthio)-4H-thieno[3,4-b][1,5]benzodiazepine | HCID 12521663 | — |
Reaction Steps
To a stirred suspension of 1.1 g. of 7-chloro-4-methyl-4,9-dihydro-10H-thieno[3,4-b] [1,5] benzodiazepin-10-thione in 15 ml. of dioxane is added dropwise and simultaneously at 30°-40°C., a solution of 1.3 g. of potassium hydroxide in 15 ml. of methanol and 1.1 g. of methyl sulfate. After addition is complete, the mixture is stirred for 3 hours, diluted with methanol and filtered. The filtrate is concentrated to 20 ml., diluted with water and the precipitate is collected. Recrystallization from methanol-water gives deep yellow crystals, m.p. 156°-158°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03951981 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-b6bb3bdf13424a74af01d68cbd31c40b |
| Source note | uspto-grants-1976_04 |