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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3222Generated: 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/3222

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 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 numberUS05733914
Source datasetuspto-grants-1998_03
ORD IDord-d3784f90e3f54ca8a6dd0f00da8e8fa4
Source noteuspto-grants-1998_03