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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9194Generated: October 29, 2026

7-Bromo-2-methoxypyrazolo[1,5-a]pyridine → 7-Bromo-2-methoxy-3-nitrosopyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/9194

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Bromo-2-methoxypyrazolo[1,5-a]pyridineHCID 21984658—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
Product7-Bromo-2-methoxy-3-nitrosopyrazolo[1,5-a]pyridineHCID 21984484—

Reaction Steps

After dissolving 7-bromo-2-methoxypyrazolo[1,5-a]pyridine (400 mg) in acetic acid (4 mL), an aqueous solution (2 mL) containing sodium nitrite (134 mg) was added and the mixture was stirred at room temperature for 30 minutes. The precipitated crystals were collected by filtration and washed with water. After dissolving the obtained crude 7-bromo-2-methoxy-3-nitrosopyrazolo[1,5-a]pyridine, without further purification, in 1,2-dimethoxyethane (40 mL) and water (20 mL), 4,6-dimethyl-2-methoxyphenylboric acid (475 mg), tetrakis(triphenylphosphine)palladium (0) complex (203 mg) and barium hydroxide octahydrate (829 mg) were added and the mixture was heated and stirred at 80° C. for 1 hour. Water was added to the reaction mixture, extraction was performed with ethyl acetate, the organic layer was washed with brine, dried over anhydrous magnesium sulfate and filtered, and the solvent was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography, and the title compound (200 mg) was obtained from the n-hexane:ethyl acetate (5:1) fraction as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091215B2
Source datasetuspto-grants-2006_08
ORD IDord-ef355f3f2c124d5b957d21085f07d951
Source noteuspto-grants-2006_08