HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → Medazepam
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Hexamethylenetetramine | HCID 4101 | — |
| Reactant | Ammonium Bromide | HCID 25514 | — |
| Reactant | 2-(2-Ethyl-methylamino)-5-chlorobenzophenone | HCID 57101088 | — |
| Solvent | Water | HCID 962 | — |
| Product | Medazepam | HCID 4041 | — |
Reaction Steps
Reflux 0.005 moles of 2-(2-ethyl-methylamino)-5-chlorobenzophenone, 0.020 moles of hexamethylenetetramine and 0.020 moles of ammonium bromide together for 2 hours in 14 ml. of 85% (v/v) aqueous isopropyl alcohol. Pour the reaction mixture into water and extract the product with benzene. Wash the benzene solution with water, dry over anhydrous sodium sulfate, filter and evaporate to dryness. After recrystallization, 7-chloro-2,3-dihydro-1-methyl-5-phenyl-1H-1,4-benzodiazepine is obtained. The material gives a single spot by thin layer chromatography, and after drying under vacuum at 110° C., shows no depression on mixed melting point with an authentic sample.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04155904 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-5985d48a684e429081cc14650201402b |
| Source note | uspto-grants-1979_05 |