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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721476Generated: October 30, 2026

4-Amino-2,2,6,6-tetramethylpiperidine → HCID 21890012, compound

https://huagongshe.com/reaction/721476

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-2,2,6,6-tetramethylpiperidineHCID 37524—
ReactantTriphosgeneHCID 94429—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(6,7-Dimethoxyquinazolin-4-yloxy)anilineHCID 11616363—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
ProductHCID 21890012HCID 2189001241%

Reaction Steps

Chloroform (10 ml) and triethylamine (2 ml) were added to 4-[(6,7-dimethoxy-4-quinazolinyl)oxy]aniline (100 mg) to prepare a solution. Triphosgene (110 mg) was added to the solution, and the mixture was stirred at room temperature for 30 min. 4-Amino-2,2,6,6-tetramethylpiperidine (79 mg) was then added thereto, and the mixture was stirred at room temperature overnight. A saturated aqueous sodium hydrogencarbonate solution was added to the reaction solution, and the mixture was extracted with chloroform. The extract was washed with saturated brine and was then dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by thin-layer chromatography using chloroform/methanol for development. Diethyl ether was added to the purification product, and the precipitated crystal was collected by filtration and was washed to give the title compound (66 mg, yield 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-195a234c58fa4afcba1fa1b83c1a5f14
Source noteuspto-grants-2006_11