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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443083Generated: October 31, 2026

Ethanol → 4-Chloro-2-methyl-7-pyridin-3-yl-thiazolo[4,5-c]pyridine

https://huagongshe.com/reaction/1443083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant3-Pyridinylboronic acidHCID 2734378—
Reactant4-Chloro-7-iodo-2-methylthiazolo[4,5-c]pyridineHCID 76850478—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product4-Chloro-2-methyl-7-pyridin-3-yl-thiazolo[4,5-c]pyridineHCID 86612415—

Reaction Conditions

Temperature80 °C

Reaction Steps

Tetrakis(triphenylphosphine)palladium(0) (52 mg, 0.05 mmol) was dissolved in 8 ml toluene. 4-Chloro-7-iodo-2-methyl-thiazolo[4,5-c]pyridine (280 mg, 0.90 mmol) (Example B), 3-pyridineboronic acid (133 mg, 1.08 mmol), 2M sodium carbonate (2.70 ml, 5.4 mmol) and 2 ml ethanol were added and the mixture stirred at 80° C. for 6 hrs. The reaction mixture was extracted with water and two times ethyl acetate. The organic extracts were washed with water and brine, dried with sodium sulfate, filtered and evaporated. The crude product was purified by flash chromatography on silica gel (heptane/ethyl acetate 9:1->0:100 gradient). The desired compound was obtained as a light yellow solid (100 mg, 42%), MS: m/e=263.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659401B2
Source datasetuspto-grants-2010_02
ORD IDord-0bc404bf89b5471684ed443d92501cf1
Source noteuspto-grants-2010_02