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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536845Generated: October 26, 2026

Diethyl Ether → 3-(4-Chloro-6-morpholin-4-yl-[1,3,5]triazin-2-yloxy)-8-methyl-8-azabicyclo[3.2.1]octane

https://huagongshe.com/reaction/536845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant8-Methyl-8-azabicyclo(3.2.1)octan-3-olHCID 8424—
Reactant2,4-Dichloro-6-morpholino-1,3,5-triazineHCID 81076—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Chloro-6-morpholin-4-yl-[1,3,5]triazin-2-yloxy)-8-methyl-8-azabicyclo[3.2.1]octaneHCID 8723960742%

Reaction Conditions

Temperature-78 °C

Reaction Steps

In a three neck flask equipped with stirring bar under N2 atmosphere tropine (1 g, 4.24 mmol) was suspended in (anhydrous) THF (15 mL). The mixture was cooled to −78° C. and BuLi (2M in THF) (5.53 ml, 1.2 eq) was added dropwise and the mixture was allowed to warm to 25° C. over 30 minutes. To the reaction mixture 2,4,-dichloro-6-morpholin-4-yl-[1,3,5]triazine (996 mg, 4,24, mmole) was added and allowed to stir overnight. For work up, ether (100 mL) was added. The organic layer was washed with water (20 mL) and brine (20 mL) and dried over MgSO4. filtered and the solvents were removed to obtain a colorless oil. Further purification by flash-chromatography using CH2Cl2/MeOH/NH3 (15:1:0.1) gave the product as white solid (600 mg, 42% yield); MS (ESI) m/z 340

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859542B2
Source datasetuspto-grants-2014_10
ORD IDord-800f0c32dc1e4ce7be79cc3341a1f392
Source noteuspto-grants-2014_10