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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433220Generated: November 3, 2026

Ethanolamine → N-(2-hydroxy-ethyl)-2-[2-(4-trifluoromethyl-phenoxymethyl)-1H-benzoimidazol-5-yl]-benzamide

https://huagongshe.com/reaction/1433220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant2-[2-(4-trifluoromethyl-phenoxymethyl)-1H-benzoimidazol-5-yl]-benzoic acidHCID 178524279—
SolventDimethylformamideHCID 6228—
ProductN-(2-hydroxy-ethyl)-2-[2-(4-trifluoromethyl-phenoxymethyl)-1H-benzoimidazol-5-yl]-benzamideHCID 17852343978%

Reaction Steps

A mixture of 2-[2-(4-trifluoromethyl-phenoxymethyl)-1H-benzoimidazol-5-yl]-benzoic acid (0.050 g, 0.121 mmol), BOP (0.059 g, 0.133 mmol), DIPEA (0.07 mL, 0.363 mmol) and ethanolamine (0.011 g, 0.182 mmol) in DMF (0.5 mL) was stirred at rt for 12 hours. The crude product was purified by chromatography (silica, CH2Cl2: MeOH, 5:1) to afford the title compound as a brown oil (0.043 g, 78%). 1H NMR (400 MHz, CD3OD) δ (ppm): 7.64-7.59 (m, 3H), 7.54-7.46 (m, 4H), 7.41 (td, 1H, J=8.2 Hz, J=1.6 Hz), 7.35 (dd, 1H, J=8.0 Hz, J=1.6 Hz), 7.15 (d, 2H, J=8.0 Hz), 5.42 (s, 2H), 5.24 (s, 1H), 3.91 (t, 2H, J=6.0 Hz), 3.24 (t, 2H, J=6.2 Hz). Mass Spectrum (LCMS, ESI pos.) Calcd. For C24H21F3N3O3: 456.4 (M+H), Found 456.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612211B2
Source datasetuspto-grants-2009_11
ORD IDord-c7b94cf407ab4d61b5dd56dbd8d9228a
Source noteuspto-grants-2009_11