Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 16115786 | HCID 16115786 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68691015 | HCID 68691015 | 39% |
Reaction Steps
To a stirring solution of lithium aluminum hydride (1.12 mL, 1.12 mmol; 1.0 M in THF) in dry tetrahydrofuran (1.2 mL) at 0° C. was added dropwise sulfuric acid (0.50 mL, 0.50 mmol; 1.0 M in THF). After 1 h, N-(t-butoxycarbonyl)-(R)-1,3,4,10b-tetrahydro-7-trifluoromethyl-pyrazino[2,1-a]isoindol-6(2H)-one (100 mg, 0.28 mmol) was added dropwise as a solution in tetrahydrofuran (1.2 mL). The reaction was slowly allowed to warm to room temperature over a period of 1 h and was then quenched by the addition of water (2 mL) and 1N aqueous sodium hydroxide (0.30 mL). The mixture was extracted with ethyl acetate (×3), and the combined organic layers were dried over sodium sulfate, filtered, and concentrated. The resulting pale yellow residue was purified by radial chromatography (30–50% ethyl acetate in hexanes) to afford N-(t-butoxycarbonyl)-(R)-1,3,4,10b-tetrahydro-7-trifluoromethyl-pyrazino[2,1-a]isoindole (37 mg, 39%) as a clear residue. MS (ESI) 343.4 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07244843B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-7b892a01734e47d783d556b50c75d45c |
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| Source note | uspto-grants-2007_07 |
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