HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → Benzodiazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | N-Methylcyclopropanamine | HCID 11029756 | — |
| Reactant | 8-nitro-1-(chloromethyl)-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine | HCID 23337467 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzodiazepine | HCID 134664 | — |
Reaction Steps
In the manner given in Example 2, potassium iodide and 8-nitro-1-(chloromethyl)-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine in tetrahydrofuran are treated with methylcyclopropylamine to give 8-nitro-1-[(cyclopropylmethylamino)methyl]-6-(o-chlorophenyl)-4H-s-triazolo[4,3-]1,4]benzodiazepine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04021441 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-67ba7fc619534de3aa356313d79962a9 |
| Source note | uspto-grants-1977_05 |