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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438024Generated: October 29, 2026

Dichloromethane → HCID 57941514, compound

https://huagongshe.com/reaction/1438024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant4-Fluoro-2-(trifluoromethyl)benzyl bromideHCID 2737576—
Reactant(4s,7r)-2-(2,4-Difluoro-phenyl)-7,8,8-trimethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-oneHCID 57941339—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 57941514HCID 5794151440%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of (4S,7R)-2-(2,4-difluoro-phenyl)-7,8,8-trimethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one (Intermediate 14; 100 mg, 0.33 mmol), tetrabutylammonium iodide (120 mg, 0.32 mmol) and 4-fluoro-2-(trifluoromethyl)benzyl bromide (204 μL, 1.3 mmol) in dimethylformamide (2 mL) was heated at 100° C. overnight. Dichloromethane (50 mL) was added and the solution was washed with 1:1 water/brine (2×25 mL), aqueous sodium thiosulfate, water, and brine. The solution was dried (magnesium sulfate), filtered, evaporated, and purified by column chromatography, eluting with 50% ethyl acetate/petroleum ether, to give an orange oil. 1H NMR showed that this oil contained some dimethyl formamide. The oil was dissolved in ethyl acetate and the solution was washed with water (3×10 mL), dried (magnesium sulfate), filtered, evaporated, then co-evaporated with ethyl ether and dichlormethane, and held under high vacuum to give (4S,7R)-2-(2,4-difluoro-phenyl)-1-(4-fluoro-2-trifluoromethyl-benzyl)-7,8,8-trimethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one (63 mg, 40%) as a pale foam. APCI(+)-MS (M+H) 481.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622492B2
Source datasetuspto-grants-2009_11
ORD IDord-5fcd35cc4f7a4fa99a8859d239304dcc
Source noteuspto-grants-2009_11