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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375773Generated: October 25, 2026

n-Butyl-2,2,6,6-tetramethyl-4-piperidinamine → Ethyl N-[2,4-bis(N-butyl-N-(2,2,6,6-tetramethyl-4-piperidyl)amino)-1,3,5-triazin-6-yl]glycinate

https://huagongshe.com/reaction/375773

Reaction equation

Participants

RoleNameHCIDCharge
Reactantn-Butyl-2,2,6,6-tetramethyl-4-piperidinamineHCID 118285—
ReactantSodium BicarbonateHCID 516892—
Reactant4,6-dichloro-2-ethoxycarbonylmethylamino-S-triazineHCID 14746261—
SolventO-XyleneHCID 7237—
ProductEthyl N-[2,4-bis(N-butyl-N-(2,2,6,6-tetramethyl-4-piperidyl)amino)-1,3,5-triazin-6-yl]glycinateHCID 1474620696.3%

Reaction Steps

2.36 g of ethyl N-(2,4-dichloro-1,3,5-triazin-6-yl)glycinate [obtained as described in Preparation 4(A)], 4.19 g of 2,2,6,6-tetramethyl-4-(butylamino)piperidine [obtained as described in Preparation i(A)] and 2.77 g of sodium bicarbonate were heated under reflux in 20 ml of xylene for 29 hours. At the end of this time, the xylene was removed by distillation under reduced pressure, and a mixture of methylene chloride and water was added to the resulting residue, after which the mixture was shaken. The methylene chloride layer was separated, dried and concentrated by evaporation under reduced pressure, and the resulting residue was purified by silica gel column chromatography (using a 20:10:1:1 by volume mixture of hexane, diethyl ether, ethanol and triethylamine as eluent), to yield 5.46 g of the title compound melting at 40° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05486556
Source datasetuspto-grants-1996_01
ORD IDord-4b2376a98a4048179b6e95cb7445ec51
Source noteuspto-grants-1996_01