HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 3-bromo-11H-s-triazolo[3,4-b][3]benzazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 11H-s-triazolo[3,4-b][3]benzazepine | HCID 21223435 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-bromo-11H-s-triazolo[3,4-b][3]benzazepine | HCID 21323390 | — |
Reaction Steps
To 1.83 g of 11H-s-triazolo[3,4-b][3]benzazepine in 40 ml of chloroform was added 0.1 ml of pyridine and 0.55 ml of bromine was added dropwise under stirring. The mixture was stirred for 2 hours, after which it was washed with water and dried over Na2SO4. After evaporation of the solvent, the residue was treated with ether. By the above procedure was obtained 3-bromo-11H-s-triazolo[3,4-b][3]benzazepine as crystals. These crystals were recrystallized from ethanol and methanol in the order mentioned to obtain pale-brown platelets melting at 169°-170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04150139 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-5ac996d1a0bb4c88a8f67848b3ed218b |
| Source note | uspto-grants-1979_04 |