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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712727Generated: November 4, 2026

HCID 23582736, compound → HCID 23582737, compound

https://huagongshe.com/reaction/1712727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23582736HCID 23582736—
ReactantHCID 178418348HCID 178418348—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23582737HCID 2358273739%

Reaction Steps

To a solution of (R)-1-(1-(3-acetyl-5-fluorophenyl)-1-(4-fluoro-3-(trifluoromethyl)phenyl)-2-phenylethyl)-3-(2,2,2-trifluoroethyl)urea (Example 257, 20 mg, 0.037 mmol) in THF (1 mL) at 0° C. under argon was added dropwise CH3Li (1.4 M in Et2O, 0.04 mL, 0.056 mmol.). The reaction mixture was stirred at room temperature for 2 h, then quenched with sat. NH4Cl and 0.5 N HCl and the aqueous layer was extracted with EtOAc. The combined organic portions were washed with H2O, sat. NaCl, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography (silica gel, hexanes/EtOAc) to give (R)-1-(1-(4-fluoro-3-(trifluoromethyl)phenyl)-1-(3-fluoro-5-(2-hydroxypropan-2-yl)phenyl)-2-phenylethyl)-3-(2,2,2-trifluoroethyl)urea (Example 258, 8 mg, yield 39%). LCMS: RT=3.89 min [M+H] 559.4 (Phenomenex Luna C18 column, 4.6×50 mm eluting with 10-90% MeOH/H2O over 4 minutes containing 0.1% NH4Cl; 4 mL/min, monitoring at 220 nm). 1H NMR (400 MHz, CDCl3) ppm 7.51-7.45 (m, 2H), 7.21-6.96 (m, 6H), 6.68 (d, J=6.8 Hz, 2H), 6.61 (d, J=9.9 Hz, 1H), 5.43 (s, br, 1H), 5.17 (m, 1H), 4.01 (d, J=13.2 Hz, 1H), 3.85-3.62 (m, 3H), 1.46 (s, 3H), 1.44 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790770B2
Source datasetuspto-grants-2010_09
ORD IDord-4aa2988dafc6403e98d45e974632260e
Source noteuspto-grants-2010_09