HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 21450905, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Propargylamine | HCID 239041 | — |
| Reactant | HCID 20291813 | HCID 20291813 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21450905 | HCID 21450905 | — |
Reaction Steps
In the manner given in Preparation 19, 8 -chloro-1-(chloromethyl)-6-(2,6-difluorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine in dimethylformamide is reacted at room temperature with propargylamine in the presence of potassium iodide to give 8-chloro-1-[[(2-propynyl)amino]methyl]-6-(2,6-difluorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine. Preparation 24 8 -Nitro-1-[[(2-propynyl)amino]methyl]-6(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04010177 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-ca405b83ae2747219f42870d1b99210c |
| Source note | uspto-grants-1977_03 |