HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 14032637, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 14032585 | HCID 14032585 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 14032637 | HCID 14032637 | 43.8% |
Reaction Steps
To a mixture of cyanogen bromide (5.76 g, 0.054 moles) and K2CO3 (8.82 g, 0.064 moles) in dimethylsulfoxide (110 ml) was added 3-(1-methyl-4-piperidinyl)-1-phenyl-1H-indazole (14.8 g, 0.051 moles) of Example 66 in dimethylsulfoxide (DMSO) (15 ml). The reaction was stirred at ambient temperature for 16 hours and then poured into water and extracted with ether. A precipitate formed in the ether which was collected and then the ether was concentrated to yield additional product. The crude product (11.5 g) was recrystallized three times from isopropyl alcohol which yielded 6.75 g (37%) of 4-(1-phenyl-1H-indazol-3-yl)-piperidine-1-carbonitrile, m.p. 124°-125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04670447 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-986459d01b914cff90aef8c2e6691b30 |
| Source note | uspto-grants-1987_06 |