HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 19994642, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-fluoro-3-piperazin-1-yl-1H-indazole | HCID 9815871 | — |
| Reactant | 3-(4-Bromobutyl)-5,5-dimethyl-4-thiazolidinone | HCID 10611772 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19994642 | HCID 19994642 | 34.6% |
Reaction Steps
To a stirred mixture of 6-fluoro-3-(1-piperazinyl)-1H-indazole (4.4 g), K2CO3 (2.8 g), 3-(4-bromobutyl)-5,5-dimethyl-4-thiazolidinone (6.6 g) and dimethylformamide (75 ml) was heated at 75° for 4 hours. The reaction was poured into H2O, and the aqueous mixture extracted with ethyl acetate. The ethyl acetate was washed (H2O), dried (MgSO4) and the solvent concentrated to afford an oil. Upon standing the oil crystallized, and when the mass was triturated with ether, 3.3 g of a solid was collected. The compound was recrystallized from toluene-hexane to yield 2.8 g of 3-(4-(1-[6-fluoro-1H-indazol-3-yl]-4-piperazinyl)-butyl)-5,5-dimethyl-4-thiazolidinone, m.p. 123°-125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05041445 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-62d0baf7b8bd4f2b85222b78258137da |
| Source note | uspto-grants-1991_08 |