Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 23091680 | HCID 23091680 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ammonia | HCID 222 | — |
| Product | HCID 11494529 | HCID 11494529 | 106.1% |
Reaction Steps
A solution of N-ethyl-N-({4-[4-(3-pyrrolidin-1-ylpropoxy)phenyl]tetrahydro-2H-pyran-4-yl}methyl)acetamide (119 mg, 0.307 mmol) in tetrahydrofuran (1 mL) was added dropwise at 0° C. to a solution of LiAlH4 (1.0M in diethylether, 0.614 mL, 0.614 mmol) under an atmosphere of nitrogen. The reaction mixture was allowed to warm to ambient temperature overnight. The reaction mixture was cooled to 0° C., water (0.5 mL) was then added dropwise followed by sodium hydroxide (2.0M, 0.5 mL) and water (0.5 mL) again. The resulting solid was filtered over a small pad of celite, washed with DCM (100 mL) and concentrated in vacuo. The compound was purified by column chromatography on Biotage® silica gel, eluting with dichloromethane:methanol:ammonia, 94.5:5.5:0.55 to 91:9:0.9 to give the title compound as a pale yellow oil (61 mg, 53%). 1H NMR (400 MHz, CDCl3) δ 7.18 (d, 2H), 6.86 (d, 2H), 4.02 (t, 2H), 3.70-3.78 (m, 2H), 3.48 (dt, 2H), 2.64 (t, 2H), 2.58-2.46 (m, 4H), 2.38 (s, 2H), 2.20 (quartet, 4H), 2.13-1.96 (m, 4H), 1.92-1.86 (m, 2H), 1.82-1.78 (m, 4H), 0.82 (t, 6H); HRMS (ESI+) 375.3006 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07456164B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-343bd8de2d124be2a74fa611f5c143fb |
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| Source note | uspto-grants-2008_11 |
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