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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014119Generated: October 31, 2026

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

https://huagongshe.com/reaction/1014119

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 numberUS07982036B2
Source datasetuspto-grants-2011_07
ORD IDord-fc9fa44a80374a8fab24aec388ce25b7
Source noteuspto-grants-2011_07