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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875050Generated: November 1, 2026

Diisopropylethylamine → 4-chloro-N-{[4-chloro-2-fluoro-3-(1-naphthalenyloxy)phenyl]methyl}-2-ethyl-1H-imidazole-5-carboxamide

https://huagongshe.com/reaction/1875050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant{[4-Chloro-2-fluoro-3-(1-naphthalenyloxy)phenyl]methyl}amineHCID 68486009—
ReactantHCID 178437661HCID 178437661—
SolventDimethylformamideHCID 6228—
Product4-chloro-N-{[4-chloro-2-fluoro-3-(1-naphthalenyloxy)phenyl]methyl}-2-ethyl-1H-imidazole-5-carboxamideHCID 17843765328.5%

Reaction Steps

HATU (0.113 g, 0.298 mmol) was added to a solution of {[4-chloro-2-fluoro-3-(1-naphthalenyloxy)phenyl]methyl}amine (0.060 g, 0.199 mmol) and 4-chloro-2-ethyl-1H-imidazole-5-carboxylic acid (0.035 g, 0.199 mmol) and diisopropylethylamine (0.052 mL, 0.298 mmol) in DMF (1 mL). The mixture was stirred at room temperature for 1 hr. The reaction mixture was extracted with ethyl acetate and water. The organic layer was washed with water and brine, dried over sodium sulfate and concentrated. The residue was purified by reverse phase HPLC (acetonitrile:water with 0.1% TFA) to give the title compound (0.026 g, 26%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.28-8.39 (m, 1H), 8.09-8.22 (m, 1H), 7.98 (dd, 1H), 7.57-7.69 (m, 3H), 7.51 (dd, 1H), 7.27-7.40 (m, 2H), 6.52 (d, 1H), 4.52 (d, 2H), 2.59 (q, 2H), 1.16 (t, 3H). ES MS: m/z 458 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-ffee3d2094e6454da351d4387ee1d44b
Source noteuspto-grants-2012_11