HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850680Generated: November 2, 2026
Trifluoroacetic acid → HCID 90411374, compound
https://huagongshe.com/reaction/1850680
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 131732451 | HCID 131732451 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 90411374 | HCID 90411374 | 98% |
Reaction Steps
To a suspension of tert-butyl 1-[4-[(2-amino-6-fluoro-pyrazolo[1,5-a]pyrimidine-3-carbonyl)amino]-3-pyridyl]piperidine-4-carboxylate trifluoroacetic acetate (prepared according to a methodology similar to the one described in Example 1) (101 mg, 0.1773 mmol) in DCM (5 mL) was added TFA (1 mL, 12.98 mmol). The mixture was stirred at room temperature for 20 hours. The solvent was removed in vacuo and the residue azeotroped with DCM (×2) and diethyl ether (×2) to give title compound as a beige solid (98% Yield, di-TFA salt). 1H NMR (500 MHz, DMSO) δ 11.10 (s, 1H), 9.58 (dd, 1H), 8.91 (d, 1H), 8.86 (d, 1H), 8.68 (s, 1H), 8.56 (d, 1H), 6.92 (s, 2H), 3.10 (d, 2H), 2.99-2.82 (m, 2H), 2.53-2.50 (m, 1H), 2.15-1.93 (m, 4H); 19F NMR (471 MHz, DMSO) δ −74.10, −151.83; LC-MS ES+: 400.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957078B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-f85a41b2c803401c8e42fcf3e1b089c8 |
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| Source note | uspto-grants-2015_02 |
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