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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778728Generated: October 31, 2026

Dichloromethane → 6-(3,5-dimethoxyphenyl)-1H-pyrazolo[4,3-c]pyridine

https://huagongshe.com/reaction/1778728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium CarbonateHCID 10340—
Reactant(3,5-Dimethoxyphenyl)boronic acidHCID 4374257—
Reactant6-Chloro-1H-pyrazolo(4,3-c)pyridineHCID 56932109—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product6-(3,5-dimethoxyphenyl)-1H-pyrazolo[4,3-c]pyridineHCID 8672283497.9%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 6-chloro-1H-pyrazolo[4,3-c]pyridine (500 mg, 3.2 mmol) (Frontier Cat. No. Z13659), (3,5-dimethoxyphenyl)boronic acid (890 mg, 4.9 mmol) (TCI Cat. No. D3513), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) complexed with dichloromethane (1:1) (200 mg, 0.3 mmol), and sodium carbonate (1.0 g, 9.8 mmol) in 1,2-dimethoxyethane (4 mL) and water (0.6 mL) was degassed, and sealed. The mixture was stirred at 110° C. overnight. After cooling it was partitioned between ethyl acetate and water. After separation the aqueous solution was extracted with ethyl acetate twice. The combined organic layers were dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by flash chromatography on a silica gel column with ethyl acetate in hexanes (0-50%) to afford the desired product (0.80 g). LCMS (M+H)+=256.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266892B2
Source datasetuspto-grants-2016_02
ORD IDord-35527c755cd047abb2356af9b4c971a4
Source noteuspto-grants-2016_02