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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75450Generated: October 30, 2026

Triethylamine → 3-(2-Chloro-6-trifluoromethyl-pyrimidin-4-yl)-8-oxa-3-aza-bicyclo[3.2.1]octane

https://huagongshe.com/reaction/75450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4-Dichloro-6-(trifluoromethyl)pyrimidineHCID 334203—
Reactant8-Oxa-3-aza-bicyclo(3.2.1)octane hydrochlorideHCID 21983536—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
Product3-(2-Chloro-6-trifluoromethyl-pyrimidin-4-yl)-8-oxa-3-aza-bicyclo[3.2.1]octaneHCID 86665901120.2%

Reaction Steps

A solution of crude 2,4-dichloro-6-(trifluoromethyl)pyrimidine (62, 6.7 mmol) in diethyl ether (10 mL) was diluted with ethanol (25 mL) and cooled in an ice-water bath. 8-Oxa-3-azabicyclo[3.2.1]octane hydrochloride (2, 3.4 mmol) was added, followed by triethylamine (2 mL). Two additional portions of 8-oxa-3-azabicyclo[3.2.1]octane hydrochloride (2, 100 mg each) were added, the mixture was slowly warmed to room temperature and stirred overnight. Additional triethylamine (4 mL) was added to the mixture, which was then concentrated to dryness under reduced pressure. The residue was purified via flash silica gel chromatography (40% ethyl acetate/hexanes) to provide the title compound as a light colored solid (1.2 g, 61%). MS (ES+): 294.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835429B2
Source datasetuspto-grants-2014_09
ORD IDord-388ffe1582cc46c48dd18fce67d6cdc3
Source noteuspto-grants-2014_09