HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 89524959, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 131732670 | HCID 131732670 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 89524959 | HCID 89524959 | — |
Reaction Steps
A solution of (2-{(chloroacetyl) [2-(3-cyano-4-fluorophenyl)ethyl]amino}ethyl)carbamate (0.12 g, 0.31 mmol) and TFA in 5 mL of DCM was stirred at room temperature for 1 h. The solvent was evaporated. The residue was dissolved in 40 mL of ethanol and K2CO3 (0.13 g, 0.93 mmol) was added. The resulting mixture was refluxed under N2 overnight, cooled to room temperature, and filtered. The filtrate was evaporated and the residue was purified with preprep-HPLC to give 2-Fluoro-5-[2-(2-oxopiperazin-1-yl)ethyl]benzonitrile. 1H-NMR (400 MHz, CDCl3) δ: 7.41˜7.44 (m, 2H), 7.07˜7.12 (m, 1H), 3.51˜3.53 (m, 4H), 3.18˜3.22 (m, 2H), 2.99˜3.04 (m, 2H), 2.75˜2.86 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08999990B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-257a6a8b33a0491eb0138db440bc64fa |
| Source note | uspto-grants-2015_04 |