HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → Benzophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 6-phenyl-4H-s-triazolo[4,3-a][1,4-]benzodiazepine | HCID 12562518 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | Benzophenone | HCID 3102 | — |
Reaction Steps
In the manner given in Example 1, 8-chloro-1-[[ (2-propynyl)amino]3-[-6-phenyl-4H-s-triazolo[4,3-a][1,4-]benzodiazepine is heated in formic acid with aqueous formaldehyde to give 5-chloro-2-[3[(2-propynyl)methylamino]methyl]-5-[(dimethylamino)methyl]-4H-1,2,4-triazol-4-yl]benzophenone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04010177 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-66eaf92fcc644df7b3865447145d3ed9 |
| Source note | uspto-grants-1977_03 |