HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648346Generated: October 27, 2026
Sodium hydride → 2-(2-Bromo-5-nitrophenyl)-4-[[2'-(N-t-butylsulfamoyl)-3-fluorobiphenyl-4-yl]methyl]-2,4-dihydro-5-ethyl-3H-1,2,4-triazol-3-one
https://huagongshe.com/reaction/1648346
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4'-(Bromomethyl)-N-t-butyl-3'-fluoro-2-biphenylsulfonamide | HCID 10046521 | — |
| Reactant | 2-(2-Bromo-5-nitrophenyl)-2,4-dihydro-5-ethyl-3H-1,2,4-triazol-3-one | HCID 135503625 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-Bromo-5-nitrophenyl)-4-[[2'-(N-t-butylsulfamoyl)-3-fluorobiphenyl-4-yl]methyl]-2,4-dihydro-5-ethyl-3H-1,2,4-triazol-3-one | HCID 10077767 | 88% |
Reaction Steps
A mixture of 2.00 g (6.39 mmol) of 2-(2-bromo-5-nitrophenyl)-2,4-dihydro -5-ethyl-3H-1,2,4-triazol-3-one (from Step B) and 184 mg (7.67 mmol) of sodium hydride in 7 mL of DMF was stirred at 50° C. for 3 hours. A solution of 4'-(bromomethyl)-N-t-butyl-3'-fluoro -2-biphenylsulfonamide (from Step F dissolved in 6 ml of DMF was then added and the resulting mixture was stirred at 50° C. for another 3 hours. The reaction mixture was quenched by addition of water followed by extractions with EtOAc, CH2Cl2, and MeOH. Water was removed and the organic layers were washed with brine, and dried over anhydrous Na2SO4. The entire crude product mixture thus obtained was flash chromatographed over silica gel (gradient elution using 0.5-2.0% MeOH in CH2Cl2) to afford 3.54 g (88%) of the title compound as a yellow solid (contaminated with some upper and lower Rf impurities by TLC but suitable for use in the next step without further purification), mp 223°-225° C.; mass spectrum (FAB) m/e 631, 633 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05436259 |
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| Source dataset | uspto-grants-1995_07 |
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| ORD ID | ord-0738fe7d8b8141bb99396d26718be0ee |
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| Source note | uspto-grants-1995_07 |
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