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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181479Generated: October 26, 2026

1,1'-Carbonyldiimidazole → 2-(4-butyl-2-fluoroanilino)-3,4-difluoro-N-(2-hydroxyethoxy)benzamide

https://huagongshe.com/reaction/2181479

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantEthanol, 2-(aminooxy)-HCID 3014186—
Reactant2-(4-Butyl-2-fluoroanilino)-3,4-difluorobenzoic acidHCID 22025690—
Product2-(4-butyl-2-fluoroanilino)-3,4-difluoro-N-(2-hydroxyethoxy)benzamideHCID 1015051668%

Reaction Steps

The title compound was prepared from reaction of 2-(4-butyl-2-fluoroanilino)-3,4-difluorobenzoic acid with CDI and 2-(aminooxy)ethanol by the general procedure of Example 1, Step E, then purified by flash column chromatography on silica (50% EtOAc/Hexane as eluant) to give 2-(4-butyl-2-fluoroanilino)-3,4-difluoro-N-(2-hydroxyethoxy)benzamide as a white solid (68%); m.p. (EtOAc/Hexane) 163-165° C. 1H NMR [400 MHz, (CD3)2SO] δ 11.85 (br s, 1 H), 8.74 (br s, 1 H), 7.44-7.38 (m, 1 H), 7.14-7.06 (m, 1 H), 7.06-7.01 (m, 1 H), 6.88 (dd, J=8.3, 1.1 Hz, 1 H), 6.83 (ddd, J=8.4, 8.4, 4.2 Hz, 1 H), 4.73 (br s, 1 H), 3.87 (t, J=4.8 Hz, 2 H), 3.58 (t, J=4.8 Hz, 2 H), 2.52 (t, J=7.5 Hz, 2 H), 1.57-1.48 (m, 2 H), 1.29 (sextet, J=7.3 Hz, 2 H), 0.89 (t, J=7.3 Hz, 3 H). Anal. Calcd for C17H15F3N2O3: C, 59.7; H, 5.5; N, 7.3. Found C, 59.4; H, 5.4; N, 7.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06891066B2
Source datasetuspto-grants-2005_05
ORD IDord-ee939e66eefa4f7a8592ff0913b1b0ab
Source noteuspto-grants-2005_05