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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778800Generated: November 4, 2026

Hydrochloric Acid → 6-(2,6-dichloro-3,5-dimethoxyphenyl)-3-(1-methyl-1H-pyrazol-4-yl)-1H-pyrazolo[4,3-c]pyridine

https://huagongshe.com/reaction/1778800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetyl chlorideHCID 6367—
ReactantSulfuryl chlorideHCID 24648—
Reactant6-(3,5-dimethoxyphenyl)-3-(1-methyl-1H-pyrazol-4-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[4,3-c]pyridineHCID 86722877—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product6-(2,6-dichloro-3,5-dimethoxyphenyl)-3-(1-methyl-1H-pyrazol-4-yl)-1H-pyrazolo[4,3-c]pyridineHCID 76285111—

Reaction Steps

At 0° C. to a stirring solution of 6-(3,5-dimethoxyphenyl)-3-(1-methyl-1H-pyrazol-4-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[4,3-c]pyridine (80 mg, 0.2 mmol) in methylene chloride (3 mL) was added dropwise a solution of sulfuryl chloride (31 μL, 0.38 mmol)(Acros Organics, Cat. #: 37815) in methylene chloride (1 mL). The mixture was stirred at r.t. overnight. To the mixture was added acetonitrile (2 mL) and it was stirred at r.t. for 1 h. Then, to the mixture was added another 31 μL of sulfuryl chloride and it was stirred at r.t. for 4 h. The solvent was removed under reduced pressure and the residue was treated with methylene chloride and sat'd NaHCO3 solution. After separation the aq. layer was extracted with methylene chloride. The combined organic layers were dried over Na2SO4. After filtration the filtrate was 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 an intermediate which was dissolved in methanol (3 mL), and cooled to 0° C. To the solution was added a pre-cooled HCl solution prepared from acetyl chloride (700 μL, 10 mmol) and methanol (1 mL). The mixture was stirred at r.t. for 4 h and then the solvents were removed. The residue was dissolved in methanol, and purified by RP-HPLC (pH=2) to afford the desired product (4.8 mg) as a TFA salt. LCMS (M+H)+=404.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266892B2
Source datasetuspto-grants-2016_02
ORD IDord-e81f0b5696944fd5baa0b50240d27dbe
Source noteuspto-grants-2016_02