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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577326Generated: October 26, 2026

Aluminium lithium hydride → 3-(6-(4-Phenoxyphenylamino)pyrimidin-4-ylamino)benzaldehyde

https://huagongshe.com/reaction/577326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminium lithium hydrideHCID 21226445—
ReactantN-methoxy-N-methyl-3-(6-(4-phenoxyphenylamino)pyrimidin-4-ylamino)benzamideHCID 57708272—
SolventTetrahydrofuranHCID 8028—
Product3-(6-(4-Phenoxyphenylamino)pyrimidin-4-ylamino)benzaldehydeHCID 5770823092.3%

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a stirred solution of N-methoxy-N-methyl-3-(6-(4-phenoxyphenylamino)pyrimidin-4-ylamino)benzamide (0.75 g, 1.7 mmol) in THF (10 mL) was added LAH (3.4 mL, 3.4 mmol, 1 M solution in THF) at −60° C. The reaction mixture was stirred at −60° C. for 1 h, was quenched with Na2SO4 solution (2 mL) and was extracted with ethyl acetate (10 mL). The organic layer was separated and washed with water (2 mL) and with brine solution (2 mL) and was dried over anhydrous Na2SO4. Filtration followed by concentration under reduced pressure gave a residue that was purified by column chromatography (SiO2, 60-120, chloroform/methanol, 9/1) to give 3-(6-(4-phenoxyphenylamino)pyrimidin-4-ylamino)benzaldehyde (0.6 g, 92%) as an off yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040541B2
Source datasetuspto-grants-2015_05
ORD IDord-b8b8481ada124366985a4aa2722603be
Source noteuspto-grants-2015_05