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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614953Generated: November 3, 2026

3-Aminobenzyl alcohol → {3-[(5-Chloro-4-{[3-(3-methoxyphenyl)propyl]amino}pyrimidin-2-yl)amino]phenyl}methanol

https://huagongshe.com/reaction/1614953

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminobenzyl alcoholHCID 80293—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 58467875HCID 58467875—
Solvent1,4-DioxaneHCID 31275—
Product{3-[(5-Chloro-4-{[3-(3-methoxyphenyl)propyl]amino}pyrimidin-2-yl)amino]phenyl}methanolHCID 5846791080.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 2,5-dichloro-N-[3-(3-methoxyphenyl)propyl]pyrimidin-4-amine (0.70 g, 2.2 mmol) and 3-aminobenzyl alcohol (0.38 g, 3.0 mmol) in 1,4-dioxane (19.1 mL) was added p-toluenesulfonic acid monohydrate (0.16 g, 0.82 mmol). The mixture was heated at 100° C. for 16 hours and the reaction was complete. After cooling, the mixture was filtered under vacuum. The cake was washed with cold EtOAc and then H2O to give the desired product as an off-white powder (0.71 g, 79%). LCMS for C21H24ClN4O2 (M+H)+: m/z=399.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765727B2
Source datasetuspto-grants-2014_07
ORD IDord-b81676a021b64a0180c90c92c48b8a66
Source noteuspto-grants-2014_07