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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563149Generated: October 29, 2026

Isopropanol → HCID 67004738, compound

https://huagongshe.com/reaction/563149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Pyridinylboronic acidHCID 2734378—
ReactantHCID 67005310HCID 67005310—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 67004738HCID 6700473835%

Reaction Conditions

Temperature100 °C

Reaction Steps

In an inert atmosphere, N—[(S)-1-benzyl-2-(4-benzyl-piperazin-1-yl)-2-oxo-ethyl]-N-(4-bromo-benzyl)-3-(4-trifluoromethyl-phenyl)-acrylamide (60 mg, 0.087 mmol) was dissolved in toluene (0.5 mL) followed by the addition of 3-pyridineboronic acid (11 mg, 0.087 mmol), 2M potassium carbonate solution (0.5 mL) and iso-propanol (0.5 mL). The mixture was degassed with argon for 5 min and heated to 100° C. followed by the addition of tetrakis-(triphenylphosphine)palladium (3 mg, 0.003 mmol). The mixture was stirred for 3 h at 110° C., cooled to rt again and water (1 mL) was added. The product was extracted with EtOAc (3×3 mL). The combined organic layers were evaporated to dryness and the residue was purified by prep. HPLC to give 21 mg (35%) of N—[(S)-1-benzyl-2-(4-benzyl-piperazin-1-yl)-2-oxo-ethyl]-N-(4-pyridin-3-yl-benzyl)-3-(4-trifluoromethyl-phenyl)-acrylamide. LC-MS: tR=0.85 min; [M+H]+=689.68.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067419B2
Source datasetuspto-grants-2011_11
ORD IDord-ba36d065da1d4b76afeb1656512434e3
Source noteuspto-grants-2011_11