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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | (7R,8aS)-2-benzyloctahydropyrrolo[1,2-a]pyrazin-7-ol | HCID 14914621 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 5-Fluoro-2-(trifluoromethyl)pyridine | HCID 26986205 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (7R,8aS)-2-benzyl-7-{[6-(trifluoromethyl)pyridin-3-yl]oxy}octahydropyrrolo[1,2-a]pyrazine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08648074B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-07dd8f4442104a97b832f6e043d05c52 |
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| Source note | uspto-grants-2014_02 |
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