Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79053Generated: October 29, 2026

HCID 86656242, compound → 4-(2-Fluoro-4-iodophenylamino)-1H-pyrazolo[3,4-b]pyridine 5-carboxylic acid (2-hydroxyethoxy)-amide

https://huagongshe.com/reaction/79053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86656242HCID 86656242—
SolventTrifluoroacetic acidHCID 6422—
Product4-(2-Fluoro-4-iodophenylamino)-1H-pyrazolo[3,4-b]pyridine 5-carboxylic acid (2-hydroxyethoxy)-amideHCID 4460308130%

Reaction Conditions

Temperature65 °C

Reaction Steps

4-(2-Fluoro-4-iodophenylamino)-1-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid (2-vinyloxyethoxy)-amide (346 mg, 0.57 mmol) was dissolved in TFA (5 mL) and the reaction mixture heated at 65° C. for 3 hours. The reaction mixture was concentrated in vacuo and the residue was dissolved in ethyl acetate (10 mL), washed with aqueous saturated sodium bicarbonate solution (10 mL) and the aqueous fraction extracted twice with ethyl acetate (2×10 mL). The combined organic extracts were washed with brine (20 mL), dried (MgSO4) and concentrated in vacuo. The resultant residue was subjected to flash chromatography (Si—SPE, gradient 0-10% methanol in DCM) to yield the title compound as a yellow solid (75 mg, 30%). LCMS (Method A): RT=6.67 min, [M+H]+=458. 1H NMR (DMSO-d6, 400 MHz) 13.51 (1H, s), 11.75 (1H, s), 10.38 (1H, s), 8.45 (1H, s), 7.80 (1H, dd, J=9.67, 1.86 Hz), 7.64-7.60 (1H, m), 7.30-7.21 (1H, m), 6.74 (1H, s), 4.71 (1H, s), 3.90 (2H, t, J=4.95 Hz), 3.61-3.56 (3H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841462B2
Source datasetuspto-grants-2014_09
ORD IDord-6fbdc15efc5348a0983adbdd13a8948c
Source noteuspto-grants-2014_09