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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550468Generated: October 30, 2026

Methylamine → N-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}-3-[2-(methylamino)ethoxy]-1H-pyrazolo[3,4-d]pyrimidin-4-amine

https://huagongshe.com/reaction/550468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant3-(2-chloroethoxy)-N-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}-1H-pyrazolo[3,4-d]pyrimidin-4-amineHCID 11705031—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductN-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}-3-[2-(methylamino)ethoxy]-1H-pyrazolo[3,4-d]pyrimidin-4-amineHCID 1161198014%

Reaction Conditions

Temperature120 °C

Reaction Steps

Methylamine in water (40% solution, 2 ml) was added to a suspension of 3-(2-chloroethoxy)-N-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}-1H-pyrazolo[3,4-d]pyrimidin-4-amine (prepared as described in Example 12/0.4 g, 0.89 mmol) in ethanol (4 ml) and the reaction mixture was heated at 120° C. for 5 minutes in a microwave reactor. The resulting solution was concentrated in vacuo and the residue purified by chromatography using DCM to DCM-10% methanol/7N ammonia as eluant to give the title compound as a white solid (57 mg, 14%); Mass Spectrum: 443.3 (MH+/retention time 1.5 minutes).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947676B2
Source datasetuspto-grants-2011_05
ORD IDord-1b385b2c14e34f34a397905300ffaf7f
Source noteuspto-grants-2011_05