HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362255Generated: October 31, 2026
Trifluoroacetic acid → HCID 66967104, compound
https://huagongshe.com/reaction/1362255
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 66966526 | HCID 66966526 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66967104 | HCID 66967104 | — |
Reaction Steps
Trifluoroacetic acid (0.5 mL) was added to a solution of (E)-7-{2-[methyl-(1-methyl-1H-indol-2-ylmethyl)-carbamoyl]-vinyl}-2-oxo-2,3-dihydro-1H-pyrido[2,3-b]pyrazine-4-carboxylic acid tert-butyl ester in CH2Cl2 (1 mL) at 10° C. After stirring 1 hr, volatiles were removed in vacuo and the resulting residue was dissolved in EtOAc (2 mL). Upon addition of dilute NaOH, a precipitate formed. The solid was collected by filtration, washed with water (100 mL), MeOH (50 mL), EtOAc (50 mL) and CH2Cl2 (50 mL) to afford the title compound (170 mg). 1H NMR (300 MHz, DMSO-d6) δ 10.42 and 10.33 (rotamers, 2s, br, 1H), 7.90 (m, 1H), 7.45 (m, 3H), 7.22 (m, 1H), 7.12 (m, 1H), 6.83 (d, J=15.4 Hz, 1H), 6.42 and 6.17 (rotamers, 2s, 1H), 4.98 and 4.84 (rotamers, 2s, 2H), 3.99 and 3.95 (rotamers, 2s, 2H), 3.72 and 3.68 (rotamers, 2s, 3H), 3.07 and 3.00 (rotamers, 2s, 3H). MS (ESI) m/e: 376 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07879872B2 |
|---|
| Source dataset | uspto-grants-2011_02 |
|---|
| ORD ID | ord-7f48fcf3648344f991bae2d04040bdb2 |
|---|
| Source note | uspto-grants-2011_02 |
|---|