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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805180Generated: November 2, 2026

HCID 53246296, compound → HCID 53246764, compound

https://huagongshe.com/reaction/1805180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 53246296HCID 53246296—
CatalystPalladiumHCID 23938—
ProductHCID 53246764HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354427B2
Source datasetuspto-grants-2013_01
ORD IDord-8478dc5c48a843019dd4962e73ce26c5
Source noteuspto-grants-2013_01