HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805180Generated: November 2, 2026
HCID 53246296, compound → HCID 53246764, compound
https://huagongshe.com/reaction/1805180
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 53246296 | HCID 53246296 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 53246764 | HCID 53246764 | — |
Reaction Steps
A flask charged with N-[5-benzyloxy-4-isopropyl-2-(trifluoromethyl)phenyl]-4-oxo-1H-quinoline-3-carboxamide (118 mg, 0.25 mmol) and Pd/C (12 mg, 0.11 mmol) was evacuated under vacuum, followed by purging with N2. Methanol (2 mL) was added under inert atmosphere, followed by evacuating under vacuum. The reaction was stirred overnight under an atmosphere of hydrogen, filtered through a plug of celite and concentrated to give N-[5-hydroxy-4-isopropyl-2-(trifluoromethyl)phenyl]-4-oxo-1H-quinoline-3-carboxamide. 1H NMR (400.0 MHz, DMSO-d6) δ 12.93 (s, 1H), 12.59 (s, 1H), 10.29 (s, 1H), 8.87 (s, 1H), 8.32 (dd, J=1.0, 8.1 Hz, 1H), 7.95 (s, 1H), 7.83-7.74 (m, 2H), 7.52 (t, J=8.0 Hz, 1H), 7.36 (s, 1H), 3.20 (qn, J=6.9 Hz, 1H) and 1.24-1.19 (m, 6H) ppm. LC/MS: m/z 391.36 (M+H)+ at 1.77 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354427B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-8478dc5c48a843019dd4962e73ce26c5 |
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| Source note | uspto-grants-2013_01 |
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