Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-(3-Nitropyridin-4-yl)-1,2,3,4-tetrahydroisoquinoline | HCID 68705703 | — |
| Reactant | HCID 178448414 | HCID 178448414 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68705712 | HCID 68705712 | 38.7% |
Reaction Steps
2-(3-Nitropyridin-4-yl)-1,2,3,4-tetrahydroisoquinoline (5 g, 19.58 mmol) prepared in Preparation 1 was dissolved in anhydrous tetrahydrofuran (200 ml) under a nitrogen atmosphere. 1-Methyl-1-propenyl magnesium bromide (0.5M in tetrahydrofuran solution, 80 ml, 117.5 mmol) was added at −78° C. to the solution, which was then stirred for 5 hours at −20° C. 20 ml of 20% ammonium chloride solution was added to the reaction mixture, which was then extracted with ethyl acetate (200 ml) twice. The separated organic layer was dried on anhydrous magnesium sulfate and then concentrated under reduced pressure. The resulting residue was purified with silica gel column chromatography (ethyl acetate/methylene chloride/methanol=10/10/1, (v/v/v)) to give the titled compound as a pale yellow solid (2.1 g, 25.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07642269B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-5860c3d775c546dcb6f7f7903154858a |
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| Source note | uspto-grants-2010_01 |
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