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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793930Generated: October 26, 2026

Ethanolamine → 6-(2,4-Dichloro-phenyl)-5-methylaminomethyl-2-phenyl-pyrimidin-4-ylamine

https://huagongshe.com/reaction/1793930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantMethyl iodideHCID 6328—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
Reactant4-Amino-6-(2,4-dichloro-phenyl)-2-phenyl-pyrimidine-5-carbonitrileHCID 15528298—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product6-(2,4-Dichloro-phenyl)-5-methylaminomethyl-2-phenyl-pyrimidin-4-ylamineHCID 10126134—

Reaction Steps

Under an atmosphere of argon, 9-BBN (0.348 ml of a 0.5 molar solution in hexane, 0.174 mmol) was added to a solution of 4-amino-6-(2,4-dichloro-phenyl)-2-phenyl-pyrimidine-5-carbonitrile (60 mg, 0.174 mmol) in THF (1 ml) and stirred for 2.5 h at r.t. Potassium-tert-butylate (20 mg, 0.174 mmol) was added, followed by a drop of Methyl iodide after 10 min. The mixture was stirred overnight, then ethanolamine (11 mg, 0.174 mmol) was added and the mixture was heated to 50° C. for 3 h. After cooling, the mixture was filtered, and the filtrate was evaporated. Purification of the re-dissolved (DMF, 1 ml) residue by automated, preparative HPLC (YMC CombiPrep C18 column 50×20 mm, solvent gradient 5–95% CH3CN in 0.1% TFA(aq) over 6.0 min, λ=230 nm, flow rate 40 ml/min) gave the tide compound, MS: m/e=358.9 (M+H+), (12 mg, 19%) as a foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022718B2
Source datasetuspto-grants-2006_04
ORD IDord-b508e4b49c704e21a427da89ce6fe587
Source noteuspto-grants-2006_04