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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675944Generated: October 31, 2026

Hydrochloric Acid → HCID 58539042, compound

https://huagongshe.com/reaction/1675944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant5-Methylpyridine-3-boronic acidHCID 2762708—
ReactantHCID 178428694HCID 178428694—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 58539042HCID 58539042—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of methyl 2-chloro-5-iodonicotonate (5-1, 10.85 g, 36.5 mmol) in dimethylformamide (150 mL) at 25° C. was added 3-methyl-5-pyridylboronic acid (5.0 g, 36.5 mmol), PdCl2dppf (2.67 g, 3.65 mmol) followed by cesium carbonate (41.6 g, 128 mmol) and water (6.57 mL, 365 mmol) and the system was stirred for 4 h at 25° C. The system was partitioned between water and EtOAc, and dried over magnesium sulfate. Filtration and concentration yielded a brown oil which upon purification via normal phase chromatography (0→100% EtOAc in Hx) afforded a brown semi-solid which was then tritirated with MeOH and diethylether to yield a dark tan powder. To this tan powder (0.5 g, 1.9 mmol) in dioxane (13 mL) was added 3-methylpyrazole (0.47 g, 5.7 mmol) and NaHMDS (1.9 mL, 3.81 mmol) and the system was heated to 125° C. for 20 minutes in the microwave reactor. The reaction contents were partitioned between water and EtOAc followed by purification via normal phase chromatography (20→100% EtOAc in Hx) to yield a clear oil. To this clear oil (0.31 g, 1.0 mmol) in THF (2.5 mL) and MeOH (2.5 mL) was added KOH (2.0 mL, 2.0 mmol) and stirred at 135° C. for 10 minutes in a microwave reactor. The system was then acidified using 6 N HCl to a pH of 2.0 and the solvents were azeotroped off with toluene to afford the title compound (5-2) as a bone powder. ESI+MS [M+H]+ C16H14N4O2=295.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003797B2
Source datasetuspto-grants-2011_08
ORD IDord-a050b8812c8c4447ae9df929e73c8f99
Source noteuspto-grants-2011_08