HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664187Generated: October 31, 2026
1-(2-Bromo-5-fluorophenyl)-4-methyl-1H-1,2,4-triazol-5(4H)-one → 4-Fluoro-2-(4-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl)benzonitrile
https://huagongshe.com/reaction/1664187
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(2-Bromo-5-fluorophenyl)-4-methyl-1H-1,2,4-triazol-5(4H)-one | HCID 58877843 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 4-Fluoro-2-(4-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl)benzonitrile | HCID 58877902 | 79% |
Reaction Steps
A mixture of 1-(2-bromo-5-fluorophenyl)-4-methyl-1H-1,2,4-triazol-5(4H)-one (0.484 g, 1.78 mmol), CuCN (0.319 g, 3.56 mmol), and 8 mL of NMP was subjected to microwave irradiation at 120° C. for 3 h. The brown mixture was filtered over Celite® and washed with DMF. This solution was treated with 10% aqueous NH4OH (28-30% solution) and extracted with EtOAc. The combined organic fractions were successively washed with 10% aqueous NH4OH (28-30% solution), saturated aqueous NH4Cl, water, brine and dried over Na2SO4. The resulting mixture was concentrated in vacuo and the residue was purified with a Biotage column chromatography system on silica gel with hexanes:ethyl acetate (3:7 to 2:8) gradient as the eluent to afford the title compound as a pink solid (0.305 g, 79% yield): 1H NMR (400 MHz, CDCl3) δ 7.76 (1H, dd, J=8.8, 5.8 Hz), 7.72 (1H, dd, J=9.6, 2.5 Hz), 7.64 (1H, s), 7.10 (1H, ddd, J=8.7, 7.4, 2.7 Hz), 3.40 (3H, s); LCMS (+ESI, M+H+) m/z 219.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039458B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-20c4779918bd4b6b9f4ad5610fea3b65 |
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| Source note | uspto-grants-2011_10 |
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