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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510851Generated: November 2, 2026

Chlorotrimethylsilane → 1-[4-chloro-3'-fluoro-5-methyl-6-(4H-1,2,4-triazol-4-yl)biphenyl-2-yl]ethanone

https://huagongshe.com/reaction/510851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
Reactant1,2-HydrazinedicarboxaldehydeHCID 12342—
Reactant1-(6-Amino-4-chloro-3'-fluoro-5-methylbiphenyl-2-yl)ethanoneHCID 58368430—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
Product1-[4-chloro-3'-fluoro-5-methyl-6-(4H-1,2,4-triazol-4-yl)biphenyl-2-yl]ethanoneHCID 8666678237.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

1,2-Hydrazinedicarboxaldehyde (0.095 g, 1.1 mmol) and then, drop by drop, chlorotrimethylsilane (0.69 mL, 5.4 mmol) and triethylamine (0.35 mL, 2.5 mmol) were added to a suspension of 1-(6-amino-4-chloro-3′-fluoro-5-methylbiphenyl-2-yl)ethanone (0.10 g, 0.36 mmol) in pyridine (2 mL). The mixture was heated at 100° C. overnight. Evaporation at reduced pressure of the solvent yielded a solid that was treated with water and extracted with dichloromethane. The extracts were dried over sodium sulfate and concentrated. The reside was purified on silica gel, eluting with 0 to 50% ethyl acetate in hexane, then 0 to 10% methanol in dichloromethane, to give the desired product (44 mg, 37%). LCMS calculated for C17H14ClFN3O (M+H)+: m/z=330.1. found: 330.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096600B2
Source datasetuspto-grants-2015_08
ORD IDord-ecbc05f3f6a64b069a4cd0b66f1302aa
Source noteuspto-grants-2015_08