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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542385Generated: October 29, 2026

Sodium Hydroxide → HCID 178467457, compound

https://huagongshe.com/reaction/542385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantN-(4-dimethylamino-6-ethoxypyrimidin-5-yl)-chloroacetamideHCID 20208140—
ReactantHCID 178478564HCID 178478564—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 178467457HCID 178467457—

Reaction Steps

To a mixture of 12.9 g (0.05 mol) N-(4-dimethylamino-6-ethoxypyrimidin-5-yl)-chloroacetamide and 2 g benzyltriethylammoniumchloride in 150 g of CH2Cl2 are added 8.4 g (0.055 mol) of 1-pyrazolylmethylchloride-hydrochloride. To this mixture are quickly added 25 ml of 40% NaOH, whereby the temperature rises from 18° to 32°. The mixture is then stirred for 2 hours and diluted with water. The organic phase is separated off and dried over Na2SO4. The dried solution is evaporated to give an orange oil that is chromatographed on silica gel with the aid of ethylacetate. The thus obtained yellow oil is dissolved in diethylether and crystallised in a deep-freezer. The title compound is obtained in the form of white crystals of m.p. 112°-114°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04657579
Source datasetuspto-grants-1987_04
ORD IDord-ef3746e0b2784720a0954597e16b8c31
Source noteuspto-grants-1987_04