HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylhydroxylamine → HCID 23337465, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylhydroxylamine | HCID 19463 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 23337469 | HCID 23337469 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23337465 | HCID 23337465 | — |
Reaction Steps
In the manner given in Example 1, 8-bromo-1-(chloromethyl)-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine is treated with a cold mixture of N,N-diethylhydroxylamine and sodium hydride in dimethylformamide to give 8-bromo-1-[(diethylamino)methyl]-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine, N1 -oxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04226772 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-ea09d2858bc34b11b794e98bb0ecdc4d |
| Source note | uspto-grants-1980_10 |