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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765997Generated: October 31, 2026

Toluene → HCID 58181279, compound

https://huagongshe.com/reaction/1765997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant2,6-Dichloro-3-(trifluoromethyl)pyridineHCID 1810337—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 58181279HCID 5818127974.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of tert-butyl-1-piperazine carboxylate (27.0 g, 145 mmol) and K2CO3 (40.0 g, 290 mmol) in DMSO (200 mL) were 2,6-dichloro-3-trifluoromethylpyridine (29.1 g, 135 mmol) and toluene (50 mL) added. The thick slurry was stirred at 80° C. for two hours, followed by addition of toluene (0.5 L) and water (1 L). The phases were separated and the organic phase was washed twice with water. The solvent from the dried (MgSO4) organic phase was evaporated at reduced pressure. The solid residue was recrystallized from EtOAc/heptane to give white crystals (37 g). The filtrate from the recrystallization was concentrated and the residue chromatographed on a column of silica with hexane/EtOAc (90:10) to give further 6.0 g of product (total yield 85%). Purity 99% (HPLC); mp 125° C. Anal. (C15H19ClF3N3O2) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07229997B2
Source datasetuspto-grants-2007_06
ORD IDord-e9889d16f0a948e79975aa609a51792c
Source noteuspto-grants-2007_06