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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360696Generated: November 1, 2026

Phosphorus oxybromide → HCID 178468567, compound

https://huagongshe.com/reaction/2360696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxybromideHCID 24613—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 178469359HCID 178469359—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 178468567HCID 17846856726.1%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 6-hydroxy-3-methyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid ethyl ester (13.7 g) and phosphorous oxybromide (19.5 g) in toluene (300 mL) was stirred at 110° C. for 5 h, cooled to r.t., and added dropwise into an ice cold solution of potassium acetate (18.2 g) in water (300 mL). The mixture was extracted twice with ethyl acetate, the combined organic phases were washed with brine, dried over magnesium sulfate and concentrated in vacuo. 6-Bromo-3-methyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid ethyl ester (4.6 g, 26%) were obtained. This material was dissolved in THF (60 mL), and 3,4-dihydro-2H-pyran (1.6 mL) and p-toluenesulfonic acid monohydrate (0.91 g) were added. The solution was stirred at r.t. for 48 h, then 3,4-dihydro-2H-pyran (1.6 mL) were added and the solution stirred again for 48 h. The mixture was poured into water and extracted with ethyl acetate, the organic layer was dried over magnesium sulfate and concentrated in vacuo. The residue was purified by flash chromatography (silica, heptane/ethyl acetate gradient). 2.2 g (38%) of the title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686150B2
Source datasetuspto-grants-2014_04
ORD IDord-fa660d363c3a4b2f90ea05e41348d802
Source noteuspto-grants-2014_04