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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487872Generated: October 30, 2026

Water → HCID 178432708, compound

https://huagongshe.com/reaction/1487872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
ReactantAzetidine hydrochlorideHCID 12308726—
ReactantHCID 178432707HCID 178432707—
SolventAcetonitrileHCID 6342—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178432708HCID 17843270827.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

Into a 10-mL sealed tube, was placed a solution of 4-(1-(3-(2,4-dimethyl-1H-imidazol-5-yl)-4-fluorobenzoyl)piperidin-4-yl)benzonitrile (compound 25.1, 200 mg, 0.50 mmol) in 1,4-dioxane (4 mL). Azetidine hydrochloride (50 mg, 0.53 mmol) and cesium carbonate (500 mg, 1.53 mmol) were added and the mixture was stirred for 48 h at 120° C. behind a blast shield. The mixture was cooled and the solids were removed by filtration. The filtrate was concentrated under reduced pressure and the crude product was purified by Prep-HPLC with the following conditions (1#-Pre-HPLC-001(SHIMADZU)): Column, SunFire Prep C18 OBD Column, 5 um, 19*150 mm; mobile phase, Water with 50 mmol NH4HCO3 and CH3CN (33.0% CH3CN up to 46.0% in 10 min, up to 100.0% in 3 min, down to 33.0% in 1 min); Detector, Waters 2489, 254 & 220 nm. The fractions containing pure compound were combined and lyophilized to yield 59.6 mg (27%) of the title compound as a white solid m/z (ES+) 440 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428502B2
Source datasetuspto-grants-2016_08
ORD IDord-be36e7fdd5d34255b6d6aa7582c1ff19
Source noteuspto-grants-2016_08