Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 75176179 | HCID 75176179 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 86761960 | HCID 86761960 | — |
Reaction Steps
2-(2,2,2-Trifluoroacetyl)-1,2,3,4-tetrahydroisoquinoline-6-carbaldehyde (2 g, 7.78 mmol) and piperidine (660 mg, 7.78 mmol) were dissolved in 1,2-dichloroethane (24 ml), and sodium triacetoxyborohydride (2.29 g, 10.89 mmol) was added. The reaction mixture was stirred for 15 h, then diluted with dichloromethane, and sat. sodium hydrogen carbonate solution (100 ml) was added. After phase separation, the aqueous phase was extracted with dichloromethane (3×100 ml). The combined organic phases were washed with sat. sodium chloride solution (50 ml), dried over magnesium sulfate and concentrated under vacuum. The crude product was purified by column chromatography (silica gel, ethyl acetate/dichloromethane/methanol 10:1:1+ammonia solution (25% aq.)). Yield: 1.88 g (74%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492559B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-45ab9fd4b11942d0909b92d09cea6f09 |
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| Source note | uspto-grants-2013_07 |
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