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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571840Generated: October 30, 2026

Trifluoroacetic acid → HCID 71499074, compound

https://huagongshe.com/reaction/571840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86674691HCID 86674691—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 71499074HCID 7149907451%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of trifluoroacetic acid (233 μl) in water (6 ml) was added a solution of (R)-tert-butyl 2-(4-(3-(6-chloropyridin-3-yl)ureido)-3-methylphenyl)morpholine-4-carboxylate (104 mg) in acetonitrile (2 ml). The reaction mixture was then capped and the mixture was shaken at 80° C. for 4 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: heptane/EtOAc/MeOH) to afford (R)-1-(6-chloropyridin-3-yl)-3-(2-methyl-4-(morpholin-2-yl)phenyl)urea (41 mg, 51%) as a white solid. MS (ISP): 349.1 ([{37Cl}M+H]+), 347.1 ([{35Cl}M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029370B2
Source datasetuspto-grants-2015_05
ORD IDord-dc6e038c62904ac0bb731b9d239547d2
Source noteuspto-grants-2015_05