Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192291Generated: October 30, 2026

Sodium Hydroxide → HCID 11177187, compound

https://huagongshe.com/reaction/2192291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant5-(Chloromethyl)-3-(4-chlorophenyl)-1,2-oxazoleHCID 2764056—
Reactant2-(2-Fluorophenyl)-3H-imidazo[4,5-c]pyridineHCID 13450778—
SolventDimethylformamideHCID 6228—
ProductHCID 11177187HCID 1117718776%

Reaction Steps

To a suspension of 2-(2-fluorophenyl)-3H-imidazo[4,5-c]pyridine (11.0 g, 50.0 mmoles) in DMF was added a 10% (w/v) solution of aqueous NaOH. To this solution, 5-(chloromethyl)-3-(4-chlorophenyl)isoxazole (13.68 g, 60.0 mmoles) dissolved in DMF was added. The reaction mixture was stirred at room temperature and monitored every half hour by LCMS. The reaction was stopped at 4 hours, after LCMS showed no progress between at 2 hour and 4 hour monitor points. The reaction product was triturated with first with water and then with EtoAc (3×). The material was crystallized by dissolving the material in MeOH with heat, followed by precipitation with water. This crystallization process was then repeated yielding 5-((3-(4-chlorophenyl)isoxazol-5-yl)methyl)-2-(2-fluorophenyl)-5H-imidazo[4,5-c]pyridine (15.385 g, 38 mmole) as white crystal at a yield of 74%. 1H 300 Mhz (d6-DMSO) sigma 6.02 (s, 2p); 7.13 (s, 1p); 7.26-7.35 (m, 2p); 7.43-7.52 (m, 1p); 7.56 (d, 2p); 7.84 (d, 1); 7.89 (d, 2p); 8.24 (d, 1); 8.28-8.36 (m, 1p); and 9.19 (s, 1p). LCMS data M/Z=405.31

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329727B2
Source datasetuspto-grants-2012_12
ORD IDord-96081e3055bb4552824fcc082f5eea5d
Source noteuspto-grants-2012_12