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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300053Generated: October 27, 2026

4-Ethylamino-2-phenylamino-pyrimidine-5-carboxylic acid ethyl ester → (4-Ethylamino-2-phenylamino-pyrimidin-5-yl)methanol

https://huagongshe.com/reaction/2300053

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Ethylamino-2-phenylamino-pyrimidine-5-carboxylic acid ethyl esterHCID 10660864—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(4-Ethylamino-2-phenylamino-pyrimidin-5-yl)methanolHCID 1068174339%

Reaction Steps

A solution of 4-ethylamino-2-phenylamino-pyrimidine-5-carboxylic acid ethyl ester (109 mg, 0.38 mmol) in 6 mL of tetrahydrofuran was added dropwise to a room temperature suspension of lithium aluminum hydride (35 mg, 0.92 mmol) in 5 mL of tetrahydrofuran. After 25 minutes, an additional 30 mg of lithium aluminum hydride was added, and stirring was continued for 30 minutes. The reaction was carefully quenched with 120 μL of water, 200 μL of 15% NaOH, and an additional 300 μL of water. After stirring for 1 hour, the white precipitate was removed by filtration, washing with ethyl acetate. The filtrate was concentrated in vacuo, and the crude material was purified by flash chromatography eluting with ethyl acetate to provide 36 mg (39%) of (4-ethylamino-2-phenylamino-pyrimidin-5-yl)-methanol, mp 174-176° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498163B1
Source datasetuspto-grants-2002_12
ORD IDord-aff90e95481c41a0b9ad4d181de5815c
Source noteuspto-grants-2002_12