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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203368Generated: October 31, 2026

Phosphorus oxychloride → 6-chloro-1-(3,3,4,4,4-pentafluorobutyl)-1H-pyrazolo[3,4-b]pyridine-3-carbonitrile

https://huagongshe.com/reaction/2203368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant3-cyano-1-(3,3,4,4,4-pentafluorobutyl)-1H-pyrazolo[3,4-b]pyridine 7-oxideHCID 118659125—
Product6-chloro-1-(3,3,4,4,4-pentafluorobutyl)-1H-pyrazolo[3,4-b]pyridine-3-carbonitrileHCID 89438374—

Reaction Conditions

Temperature75 °C

Reaction Steps

To the intermediate from Step A above (225 mg, 0.735 mmol) was added POCl3 (2.8 g, 18.3 mmol) and the mixture was stirred at 75° C. for 9 hours. The reaction mixture was then concentrated in vacuo to remove POCl3. To the residue was added hexane/ethyl acetate (2/1, 50 mL) and the pH adjusted to 7.5˜8.0 with aqueous K2CO3 at 0° C. The water layer was extracted with the hexane/ethyl acetate (2/1, 2×20 mL). The combined organic layer was dried over Na2SO4 and evaporated under reduced pressure. The residue was purified by silica gel column chromatography using hexane/ethyl acetate eluent to give the product as a white solid. 1H NMR (500 MHz, CDCl3): δ 2.86 (m, 2H); 4.90 (t, J=8.4 Hz, 2H); 7.42 (d, J=8.4 Hz, 1H); 8.17 (d, J=8.4 Hz, 1H), m/z=325.04 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365574B2
Source datasetuspto-grants-2016_06
ORD IDord-cf2abfcf4f2c44fa9427e5094c344faf
Source noteuspto-grants-2016_06