HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → HCID 14032617, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 14032515 | HCID 14032515 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 14032617 | HCID 14032617 | 28.2% |
Reaction Steps
A sample of 8.4 g of 1-benzoyl-3-(1-methyl-4-piperidinyl)-1H-indazole hydrochloride was converted to its free base and the base was dissolved in 135 ml of chloroform. The solution was stirred and 4.0 g of potassium carbonate was added followed by 2.7 g of cyanogen bromide. The reaction mixture was stirred under reflux for 16 hrs. The mixture was filtered, and the solvent was removed in vacuo. The mixture was chromatographed on a high-pressure column chromatography apparatus (silica gel), eluting with 0.3% methanol/dichloromethane. Evaporation of the appropriate fraction followed by recrystallization from toluene hexane yielded 2.2 g (28%) of the product, mp 144°-146° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04670447 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-d045d2d046c345218d11ba73d1506ee3 |
| Source note | uspto-grants-1987_06 |