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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339021Generated: October 28, 2026

Isopropanol → HCID 86707517, compound

https://huagongshe.com/reaction/339021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantTriethylamineHCID 8471—
ReactantCesium fluorideHCID 25953—
Reactant1,3-DIMETHYL-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1H-PYRAZOLEHCID 4912748—
ReactantHCID 86707518HCID 86707518—
CatalystCID 53485975HCID 53485975—
SolventEthyl AcetateHCID 8857—
ProductHCID 86707517HCID 8670751774%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of tert-butyl (S)-1-((R)-1-(3-(7-bromo-6-fluoro quinolin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yl)-2,2,2-trifluoroethyl)pyrrolidin-3-ylcarbamate (0.10 g, 0.16 mmol), 1,3-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (0.073 g, 0.33 mmol) and cesium fluoride (0.065 g, 0.43 mmol) in 2-propanol (3.3 mL, 0.16 mmol) was degassed with nitrogen. Maintaining a nitrogen atmosphere, triethylamine (0.034 mL, 0.25 mmol) and dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct (0.013 g, 0.016 mmol) were added, and the vessel sealed and heated at 100° C. for 17 hours. After cooling, the reaction mixture was diluted with ethyl acetate (10 mL), filtered through a plug of Celite®, and concentrated under reduced pressure. Purification of the residue by reverse phase chromatography on a C18 column (0-100% acetonitrile/water) provided the title compound (0.074 g, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889704B2
Source datasetuspto-grants-2014_11
ORD IDord-9d98199c0730446eaee034056759c44a
Source noteuspto-grants-2014_11