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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230683Generated: October 30, 2026

N,N-Dimethylglycine → 4-Morpholinyl{4-[3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}methanone

https://huagongshe.com/reaction/230683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylglycineHCID 673—
ReactantCesium carbonateHCID 10796—
Reactant4-[(4-Iodophenyl)carbonyl]morpholineHCID 772634—
Reactant3-(Trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazoleHCID 2802863—
CatalystHCID 178419072HCID 178419072—
SolventDimethyl SulfoxideHCID 679—
Product4-Morpholinyl{4-[3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}methanoneHCID 131662982%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 4-[(4-iodophenyl)carbonyl]morpholine (1.90 g, 6.0 mmol), 3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazole (1.14 g, 6.0 mmol), copper (I) oxide (10 mol %, 0.6 mmol, 86 mg), N,N-dimethylglycine (20 mol %, 1.2 mmol, 124 mg), and cesium carbonate (12.0 mmol, 3.91 g) in dimethylsulfoxide (16 ml) was stirred in an oilbath heated at 130° C. for 24 h under argon and then allowed to cool to room temperature. The reaction mixture was partitioned between dichloromethane (30 ml) and water (30 ml). The organic layer was separated and dried over sodium sulphate. The solvent was removed by rotary evaporation to give a dark brown residue that was added to a 20 g isolute pre-packed silica column and eluted from 0-50% ethyl acetate in petroleum ether to give the title compound as a brown gum (1.86 g, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566735B2
Source datasetuspto-grants-2009_07
ORD IDord-6ad4561296a5482eb86433f37de142e2
Source noteuspto-grants-2009_07