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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571827Generated: October 30, 2026

Trifluoroacetic acid → HCID 71086881, compound

https://huagongshe.com/reaction/571827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86674687HCID 86674687—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 71086881HCID 7108688161.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of trifluoroacetic acid (84 μl) in water (4.5 ml) was added a solution of tert-butyl (RS)-2-(3-cyano-4-(1-(4-fluorophenyl)-1H-pyrazole-3-carboxamido)phenyl)morpholine-4-carboxylate (41 mg) in acetonitrile (2 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 (SiO2; gradient: 0% to 10% methanol in dichloromethane) to afford (RS)—N-(2-cyano-4-(morpholin-2-yl)phenyl)-1-(4-fluorophenyl)-1H-pyrazole-3-carboxamide (20 mg, 61%) as a white solid. MS (ISP): 392.2 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029370B2
Source datasetuspto-grants-2015_05
ORD IDord-8ed397aff6b84fd58fb1be7a72e7b82a
Source noteuspto-grants-2015_05