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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571823Generated: October 31, 2026

Trifluoroacetic acid → HCID 71086792, compound

https://huagongshe.com/reaction/571823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86674685HCID 86674685—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 71086792HCID 7108679296.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of trifluoroacetic acid (200 μl) in water (4.5 ml) was added a solution of tert-butyl (RS)-2-(3-chloro-4-(1-(4-fluorophenyl)-1H-pyrazole-4-carboxamido)phenyl)morpholine-4-carboxylate (100 mg) in acetonitrile (3 ml). The reaction mixture was then capped and the mixture was shaken at 80° C. for 5 h. The reaction mixture was then cooled to room temperature and poured into 1 M aq. NaOH and the resulting mixture was extracted twice with EtOAc. The organic layers were dried over Na2SO4 and concentrated in vacuo. The crude material was purified by flash column chromatography (Isolute® Flash-NH2 from Separtis); gradient: MeOH/EtOAc/heptane) to afford (RS)—N-(2-chloro-4-(morpholin-2-yl)phenyl)-1-(4-fluorophenyl)-1H-pyrazole-4-carboxamide (77 mg, 96%) as a white solid. MS (ISP): 403.1 ([{37Cl}M+H]+), 401.0 ([{35Cl}M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029370B2
Source datasetuspto-grants-2015_05
ORD IDord-07cb2c01fa574e64a8972b9d7c037436
Source noteuspto-grants-2015_05