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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345998Generated: October 30, 2026

Diethanolamine → 2-[Bis-(2-hydroxyethyl)-amino]-4-morpholino-6-(4,4-ethylenedioxy-2,2,6,6-tetramethylpiperidin-1-yl)-1,3,5-triazine

https://huagongshe.com/reaction/345998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethanolamineHCID 8113—
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloro-4-morpholino-6-(4,4-ethylenedioxy-2,2,6,6-tetramethylpiperidin-1-yl)-1,3,5-triazineHCID 19991760—
SolventWaterHCID 962—
SolventO-XyleneHCID 7237—
Product2-[Bis-(2-hydroxyethyl)-amino]-4-morpholino-6-(4,4-ethylenedioxy-2,2,6,6-tetramethylpiperidin-1-yl)-1,3,5-triazineHCID 19991769—

Reaction Steps

5.3 g of diethanolamine and a solution of 1 g of NaOH in 3 ml of water are added to a solution of 20 g of 2-chloro-4-morpholino-6-(4,4-ethylenedioxy-2,2,6,6-tetramethylpiperidin-1-yl)-1,3,5-triazine (product from Example 44) in 50 ml of xylene. 1 g of NaOH in 3 ml of water is again added after 1.75 hours with stirring under reflux. After 14 hours, 7.9 g of diethanolamine are added, after which the mixture is stirred under reflux for a further 28 hours. It is then allowed to cool and washed with water, and the organic phase is separated off. After drying over Na2SO4, evaporating and recrystallizing twice from toluene, the above product is obtained as a white powder which melts at 135°-140°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05059689
Source datasetuspto-grants-1991_10
ORD IDord-ef585ad905df4281a6974dd7c49ff092
Source noteuspto-grants-1991_10