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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354393Generated: November 2, 2026

Trifluoroacetic acid → HCID 46941286, compound

https://huagongshe.com/reaction/2354393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylamineHCID 8471—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant1-([1,1'-Biphenyl]-4-yl)-N-methyl-2-(pyrrolidin-1-yl)ethan-1-amineHCID 2756716—
Reactant{3-oxo-6-[(trifluoromethyl)oxy]-2,3-dihydro-4H-1,4-benzoxazin-4-yl}acetic acidHCID 57488862—
SolventDimethylformamideHCID 6228—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductHCID 46941286HCID 4694128651.6%

Reaction Steps

[1-(4-biphenylyl)-2-(1-pyrrolidinyl)ethyl]methylamine (0.087 g, 0.31 mmol) and {3-oxo-6-[(trifluoromethyl)oxy]-2,3-dihydro-4H-1,4-benzoxazin-4-yl}acetic acid (0.1 g, 0.34 mmol) were dissolved in 1 mL of dimethylformamide. Triethylamine (0.13 mL, 0.93 mmol) was delivered to the room temperature mixture, and the solution was allowed to stir for several minutes before a separate solution of 1H-1,2,3-benzotriazol-1-yloxy-tris(dimethylamino)-phosphonium hexafluorophosphate (BOP reagent, 0.150 g, 0.34 mmol) dissolved in 1 mL of dimethylformamide was added at room temperature to the mixture. The reaction was maintained at that temperature for 18 hours, before it was determined to be complete by LCMS (two Aquasil C18, 20×1 mm columns were run in sequence, 4 minutes at 0.1 mL/min, 1-99% CH3CN/H2O with 0.018% trifluoroacetic acid, ES) Rt=2.0 min and m/e 554 [M+1]+. The reaction mixture was filtered through a 0.45 μm PTFE Acrodisk and the crude residue was purified by prep HPLC (Waters, 50×100 mm, 84 mL/min, A: acetonitrile B: water (pH=10, NH4OH), A: 10 to 99% over 15 min, UV detection at 214 nm) to give the title compound (0.087 g. 0.16 mmol, 46%) as an off-white amorphous solid. MS (ES) m/e 554 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07749998B2
Source datasetuspto-grants-2010_07
ORD IDord-2e4c5fe7435a447a850438e84799cf0d
Source noteuspto-grants-2010_07