HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → HCID 21543672, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Quinoline, 2-hydrazinyl- | HCID 85111 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21543672 | HCID 21543672 | — |
Reaction Steps
2-Hydrazinoquinoline (25.0 grams) was placed in a 3-liter flask (three-necked, equipped with a condenser) containing 1500 milliliters of methanol. To this flask was added 17 grams of cyanogen bromide. The reaction mixture was refluxed for six hours, at which time it was cooled. The reaction mixture was then evaporated down to approximately 200 milliliters. This solution was then poured into 1 liter of absolute ether. The precipitate which formed was washed with an aliphatic naphtha solvent. This precipitate, the desired 1 -amino-s-triazolo(4,3-a)quinoline hydrobromide, was separated by filtration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03953457 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-eb82cfe6bf6148128cddf3d8098c9086 |
| Source note | uspto-grants-1976_04 |