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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786457Generated: November 1, 2026

Water → HCID 68565359, compound

https://huagongshe.com/reaction/1786457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2,2,2-Trifluoroethyl MethanesulfonateHCID 556565—
ReactantHCID 24958567HCID 24958567—
SolventDimethylformamideHCID 6228—
ProductHCID 68565359HCID 6856535953%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 144 mg (0.26 mmol) [6-bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-(4-ethanesulfonyl-piperazin-1-yl)-methanone (example 10) in 3 mL N,N-dimethylformamide, were added 13 mg (0.29 mmol; 55% dispersion in mineral oil) sodium hydride. The reaction mixture was stirred 15 min at 70° C. 68 mg (0.29 mmol) 2,2,2-Trifluoroethyl methanesulfonate were added and the solution was stirred another 2 h at 70° C. After cooling to room temperature, the reaction was poured into water and the phases were separated. The aqueous phase was extracted three times with ethyl acetate. The combined organic layers were washed with water and brine, dried over magnesium sulfate, filtered and evaporated. The crude product was purified by flash chromatography on silica gel with dichloromethane:methanol:ammonia (9:1:0.1 v/v) as eluant, to afford 86 mg (52%) of the title compound as a light-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507736B2
Source datasetuspto-grants-2009_03
ORD IDord-664e9c5a155c430cac4fb54f62b4950a
Source noteuspto-grants-2009_03