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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778683Generated: November 1, 2026

Methanesulfonic Acid → 6-Chloro-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[4,3-c]pyridine

https://huagongshe.com/reaction/1778683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantTetrahydrofuranHCID 8028—
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactant6-Chloro-1H-pyrazolo(4,3-c)pyridineHCID 56932109—
SolventDichloromethaneHCID 6344—
Product6-Chloro-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[4,3-c]pyridineHCID 71463635112.2%

Reaction Steps

At r.t. to a suspension of 6-chloro-1H-pyrazolo[4,3-c]pyridine (0.5 g, 3 mmol) (Frontier Cat. No. Z13659) in methylene chloride (3 mL) and THF (1 mL) was added methanesulfonic acid (42 μL, 0.65 mmol), followed by dihydropyran (0.89 mL, 9.8 mmol). The mixture was stirred at r.t. for 2 h., and then at 50° C. overnight. After cooling the mixture 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 the desired product (0.8 g). LCMS (M+H)+=238.0; LCMS (M-84+H)+=154.0/156.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266892B2
Source datasetuspto-grants-2016_02
ORD IDord-7c47d81698804d49ab4c52564c4bff90
Source noteuspto-grants-2016_02