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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874901Generated: November 1, 2026

HCID 68485937, compound → 5-{[3-(Aminomethyl)-6-chloro-2-fluorophenyl]oxy}-1,3-benzenedicarbonitrile

https://huagongshe.com/reaction/1874901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68485937HCID 68485937—
ReactantHCID 178514179HCID 178514179—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-{[3-(Aminomethyl)-6-chloro-2-fluorophenyl]oxy}-1,3-benzenedicarbonitrileHCID 6848723377.8%

Reaction Conditions

Temperature120 °C

Reaction Steps

3-{[3-(aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-bromobenzonitrile (0.355 g, 0.998 mmol) was combined with dicyanozinc (0.100 g, 0.852 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.115 g, 0.100 mmol) in DMF (3 mL) and heated at 120° C. for 25 min in a microwave reactor under an inert atmosphere. The reaction mixture was diluted with EtOAc, washed twice with saturated aqueous NaHCO3 and twice with water, dried over MgSO4, filtered and concentrated to dryness. The residue was dissolved in CH3OH and gravity filtered through a StratoSpheres™ PL-Thiol MP SPE+ cartridge. The filtrate was concentrated to dryness and purified on 40 g silica gel eluted successively with EtOAc and 10% CH3OH/DCM to give 5-{[3-(aminomethyl)-6-chloro-2-fluorophenyl]oxy}-1,3-benzenedicarbonitrile (0.200 g, 0.663 mmol, 66.4% yield) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.22 (s, 1H), 7.91 (s, 2H), 7.46-7.57 (m, 2H), 3.77 (s, 2H), 1.90 (br. s., 2H). LC-MS (ES+) m/z 302.27, 304.19 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-5ade8d49ee67472983ef7af1e1f95f45
Source noteuspto-grants-2012_11