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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875456Generated: November 1, 2026

2-[3-(2-Fluorobenzyl)-1H-pyrazolo[4,3-b]pyridin-1-yl]-5-nitropyrimidine-4,6-diamine → HCID 24794429, compound

https://huagongshe.com/reaction/1875456

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[3-(2-Fluorobenzyl)-1H-pyrazolo[4,3-b]pyridin-1-yl]-5-nitropyrimidine-4,6-diamineHCID 59177873—
CatalystPalladiumHCID 23938—
SolventPyridineHCID 1049—
ProductHCID 24794429HCID 24794429—

Reaction Conditions

Temperature50 °C

Reaction Steps

690 mg (1.42 mmol) of 2-[3-(2-fluorobenzyl)-1H-pyrazolo[4,3-b]pyridin-1-yl]-5-nitropyrimidine-4,6-diamine from example 15A are dissolved in 120 ml of pyridine. 270 mg of 10% palladium on activated carbon are added, and hydrogenation is carried out under a hydrogen pressure of 3.5 bar for 15 h. The catalyst is then filtered off and washed with ethanol. The residue after concentration to dryness is stirred with ethanol at 50° C. and filtered off with suction. 378 mg (76% of theory) of the desired product are obtained. A further 92 mg (18% of theory) of the target compound can be obtained from the filtrate by purifying by preparative HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309551B2
Source datasetuspto-grants-2012_11
ORD IDord-5a0310e471ef47098f6ad1a28482e1bf
Source noteuspto-grants-2012_11