HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 59231992, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Reactant | HCID 59232204 | HCID 59232204 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59231992 | HCID 59231992 | 31.1% |
Reaction Steps
To a solution of t-butyl (4-{7-[(4-acetylpiperazin-1-yl)methyl]-4-aminopyrrolo[2,1-f][1,2,4]triazin-5-yl}-2-fluorophenyl)carbamate (320 mg, 0.62 mmol) in CH2Cl2 (8 ml) was added TFA (3 ml) and was stirred at rt for 3 h. The reaction mixture was partially evaporated and was added 10 ml ethyl acetate and washed with saturated aq. NaHCO3. The organic was dried over Na2SO4, concentrated and purified via column chromatography (95:5, v/v, CH2Cl2—CH3OH) to afford 74 mg of the title compound (yield 30%). 1H-NMR (CH3OH-d4) δ 7.85 (s, 1H), 7.10 to 7.00 (m, 3H), 6.66 (s, 1H), 4.00(s, 2H), 3.60 to 3.50(m, 4H), 2.63 to 2.55(m, 4H), 20.6(s, 3H); MS [M+H]+=383.9; LCMS RT=1.10 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143393B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-87eaca0997314d479b4428594f5e6739 |
| Source note | uspto-grants-2012_03 |