HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxylamine → 8-chloro-1-[(hydroxyamino)methyl]-6-(o-chlorophenyl)-4H-s-triazolo [4,3-a][1,4]benzodiazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 8-chloro-1-(chloromethyl)-6-(o-chlorophenyl)-4H-s-triazolo-[4,3-a][1,4]benzodiazepine | HCID 12612348 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-chloro-1-[(hydroxyamino)methyl]-6-(o-chlorophenyl)-4H-s-triazolo [4,3-a][1,4]benzodiazepine | HCID 20361235 | — |
Reaction Steps
In the manner given in Example 15, 8-chloro-1-(chloromethyl)-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine is treated with a cold mixture of hydroxylamine and sodium hydride in dimethylformamide to give 8-chloro-1-[(hydroxyamino)methyl]-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04081452 |
| Source dataset | uspto-grants-1978_03 |
| ORD ID | ord-f6fec615432649f1a8f03cfa2a02d39c |
| Source note | uspto-grants-1978_03 |