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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875021Generated: October 28, 2026

2-Dimethylaminopyridine → HCID 53327927, compound

https://huagongshe.com/reaction/875021

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-DimethylaminopyridineHCID 21885—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acidHCID 25180854—
ReactantHCID 67323950HCID 67323950—
SolventDimethylformamideHCID 6228—
ProductHCID 53327927HCID 5332792746.2%

Reaction Steps

Dimethylaminopyridine (0.151 g, 1.24 mmol), EDCl (0.142 g, 0.744 mmol), and HOBt (0.095 g, 0.620 mmol) were added to a solution of 2-(azetidin-3-ylmethyl)-4-(4-fluorophenyl)thiazole (0.170 g, 0.682 mmol) in DMF (10.0 mL), followed by 3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid (0.160 g, 0.62 mmol). The reaction was stirred at room temperature for 2 h and concentrated under reduced pressure. The residue was diluted with EtOAc, washed with water and brine, dried over anhydrous Na2SO4, and concentrated under reduced pressure to yield the crude product which was purified by preparative thin layer chromatography using (40% EtOAc/Hexane) to provide (3-((4-(4-fluorophenyl)thiazol-2-yl)methyl)azetidin-1-yl)(3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)phenyl)methanone (0.140 g, 42.04%) 1H NMR (400 MHz, DMSO) δ 8.21 (s, 1H), 8.15-8.17 (d, 1H), 7.94-7.95 (d, 1H), 7.90-7.92 (m, 2H), 7.86-7.88 (d, 1H), 7.66-7.78 (t, 1H), 7.19-7.23 (t, 2H), 4.48-4.52 (t, 1H), 4.17-4.25 (m, 2H), 3.91-3.95 (m, 1H), 3.42-3.43 (m, 2H), 3.10-3.17 (m, 1H). MS (ESI) m/z: Calculated for C23H16F4N4O2S: 488.09. found: 489.0 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981084B2
Source datasetuspto-grants-2015_03
ORD IDord-376a1d8f3d1c47ee82cb27f0a987a76f
Source noteuspto-grants-2015_03