HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972971Generated: October 30, 2026
Trifluoroacetic acid → HCID 58529315, compound
https://huagongshe.com/reaction/1972971
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 86659606 | HCID 86659606 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58529315 | HCID 58529315 | 98.5% |
Reaction Steps
To a suspension of (2-(4-[4-Amino-5-(3-amino-2-benzyl-2H-indazol-6-yl)-pyrrolo[2,1-f][1,2,4]triazin-7-yl]-piperidin-1-yl)-2-oxo-ethyl)-methyl-carbamic acid tart-butyl ester (30 mg, 0.049 mmol) in anhydrous DCM (1.0 mL) was added trifluoroacetic acid (1.0 mL), and the reaction mixture was stirred at rt. After 1 h, the mixture was poured into EtOAc (75 mL), and the organic phase was washed with aqueous, saturated NaHCO3 solution (3×25 mL), water and brine, dried over Na2SO4, filtered, and concentrated in vacuo. Trituration with DCM-hexane afforded the title compound (24.7 mg, 98.5%) as a pink solid. 1H NMR (300 MHz, DMSO-d6) δ 7.88 (s, 1H), 7.71 (d, 1H), 7.34 to 7.29 (m, 2H), 7.27 to 7.21 (m, 3H), 7.15 (s, 1H), 6.73 (dd, 1H), 6.54 (s, 1H), 6.37 (broad s, 2H), 5.38 (s, 2H), 4.50 (d, 1H), 3.90 (d, 1H), 3.42 to 3.27 (m, 3H), 3.13 (t, 1H), 2.76 to 2.66 (m, 1H), 2.26 (s, 3H), 2.05 to 1.99 (m, 3H), 1.68 to 1.49 (m, 2H); ES-MS m/z 510.1 [M+H]+, RT (min) 1.56.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08431695B2 |
|---|
| Source dataset | uspto-grants-2013_04 |
|---|
| ORD ID | ord-64fb6590d10949b6acaf6560136a23b3 |
|---|
| Source note | uspto-grants-2013_04 |
|---|