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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852911Generated: October 25, 2026

Sodium Hydroxide → 4-[(4-Pyrazin-2-yl-pyrimidin-2-ylamino)-methyl]-benzoic acid

https://huagongshe.com/reaction/852911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant(E)-3-(Dimethylamino)-1-(pyrazin-2-YL)prop-2-EN-1-oneHCID 5825354—
ReactantSodium MethoxideHCID 10942334—
Reactant4-Guanidinomethyl-benzoic acid methyl ester dihydrateHCID 178497935—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product4-[(4-Pyrazin-2-yl-pyrimidin-2-ylamino)-methyl]-benzoic acidHCID 6662216787.6%

Reaction Steps

A suspension of 24 (6.2 g, 25.4 mmol) and 23a (3.0 g, 16.9 mmol) in anhydrous methanol (40 mL) was stirred and heated to reflux for 10 min, then a solution of sodium methoxide 95% (3.65 g, 67.6 mmol) in methanol (40 mL) was slowly added. After refluxing for 24 h, 20 mL of 2.5N NaOH in water were added and the refluxing was maintained for additional 24 h. The mixture was allowed to cool to the room temperature methanol was removed under reduced pressure, 100 mL of water were added and the resultant mixture was extracted with AcOEt. The aqueous phase was separated and acidified to pH 5-6 with 2N HCl to form a precipitate which was collected by filtration, rinsed with water and dried to afford the desired carboxylic acid 25a (4.55 g, 14.8 mmol, 87%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253204B2
Source datasetuspto-grants-2007_08
ORD IDord-6fd3e27df8764876b3ae31b0ddb88e9c
Source noteuspto-grants-2007_08