HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 2-(1,4-Bis-(4-fluoro-phenyl)-1H-imidazol-2-yl)-1-(4-[1,3,5]triazin-2-yl-piperazin-1-yl)-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | 2-(Piperazin-1-yl)-1,3,5-triazine | HCID 2760673 | — |
| Reactant | (1,4-bis-(4-fluoro-phenyl)-1H-imidazol-2-yl)-acetic acid lithium salt | HCID 89620421 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(1,4-Bis-(4-fluoro-phenyl)-1H-imidazol-2-yl)-1-(4-[1,3,5]triazin-2-yl-piperazin-1-yl)-ethanone | HCID 71599772 | 64.2% |
Reaction Steps
22 mg 1-(1,3,5-triazin-2-yl)-piperazine was added to 40 mg (1,4-bis-(4-fluoro-phenyl)-1H-imidazol-2-yl)-acetic acid lithium salt, 45 mg TBTU, 0.03 mL DIPEA in 0.75 mL DMF. The reaction was stirred overnight at RT. 5 mL water was added to the reaction and the mixture was stirred 1 h. The precipitate was filtered and dried to give 37 mg desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08937176B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-0bd3b8d641e5473daa1a3b759765c740 |
| Source note | uspto-grants-2015_01 |