HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377862Generated: October 30, 2026
Ethyl trifluoroacetate → HCID 136335677, compound
https://huagongshe.com/reaction/2377862
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | N-Desmethyl Dovitinib | HCID 135543684 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 136335677 | HCID 136335677 | — |
Reaction Steps
4-Amino-5-fluoro-3-(6-piperazin-1-yl-1H-benzoimidazol-2-yl)-1H-quinolin-2-one was taken up in ethyl trifluoroacetate and N,N-dimethylacetamide (DMA). The resulting solution was heated at 130° C. in a sealed tube for 30 minutes. The reaction was cooled to room temperature and quenched by addition of saturated aqueous sodium bicarbonate followed by pouring the mixture into water. The resulting solid was collected by filtration and washed with diethyl ether to afford 4-amino-5-fluoro-3-{6-[4-(2,2,2-trifluoro-acetyl)-piperazin-1-yl]-1H-benzoimidazol-2-yl}-1H-quinolin-2-one (Rt 2.63 minutes, MH+=457.1), which was immediately taken up in THF. Borane-THF complex (3.3 equivalents) was added and the reaction was stirred at room temperature overnight. After quenching the excess borane with water, the mixture was extracted into ethyl acetate, dried over magnesium sulfate, filtered and concentrated to a brown solid which was purified by reverse phase HPLC to yield the desired compound. MH+=461.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07470709B2 |
|---|
| Source dataset | uspto-grants-2008_12 |
|---|
| ORD ID | ord-842e34216cfd4e2aa5215e748fe7769a |
|---|
| Source note | uspto-grants-2008_12 |
|---|