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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 68485937 | HCID 68485937 | — |
| Reactant | HCID 178514179 | HCID 178514179 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-{[3-(Aminomethyl)-6-chloro-2-fluorophenyl]oxy}-1,3-benzenedicarbonitrile | HCID 68487233 | 77.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08304419B2 |
|---|
| Source dataset | uspto-grants-2012_11 |
|---|
| ORD ID | ord-5ade8d49ee67472983ef7af1e1f95f45 |
|---|
| Source note | uspto-grants-2012_11 |
|---|