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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240441Generated: October 29, 2026

Tetrahydrofuran → (7R,8aS)-2-benzyl-7-{[6-(trifluoromethyl)pyridin-3-yl]oxy}octahydropyrrolo[1,2-a]pyrazine

https://huagongshe.com/reaction/240441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant(7R,8aS)-2-benzyloctahydropyrrolo[1,2-a]pyrazin-7-olHCID 14914621—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant5-Fluoro-2-(trifluoromethyl)pyridineHCID 26986205—
SolventDimethyl SulfoxideHCID 679—
Product(7R,8aS)-2-benzyl-7-{[6-(trifluoromethyl)pyridin-3-yl]oxy}octahydropyrrolo[1,2-a]pyrazineHCID 86680452—

Reaction Steps

To a solution of (7R,8aS)-2-benzyloctahydropyrrolo[1,2-a]pyrazin-7-ol (Example 19D, 0.103 g, 0.443 mmol) in dimethyl sulfoxide (4 mL) was added a 1.0 M solution of potassium tert-butoxide in tetrahydrofuran (0.665 mL, 0.665 mmol), and the resulting suspension was stirred at room temperature for 5 minutes. 5-Fluoro-2-(trifluoromethyl)pyridine (0.137 g, 0.829 mmol) was added, and the reaction mixture was stirred at room temperature for 48 hours. The mixture was partitioned between ethyl acetate and water, and the organic extract was dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. Purification by column chromatography on silica gel using a solvent gradient of 0-95% ethyl acetate in hexane gave the titled compound. MS (APCI) m/z 378.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648074B2
Source datasetuspto-grants-2014_02
ORD IDord-07dd8f4442104a97b832f6e043d05c52
Source noteuspto-grants-2014_02