Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 45275021 | HCID 45275021 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 45275133 | HCID 45275133 | 54% |
Reaction Steps
To a solution of N-(2-aminoethyl)-1-(3,5-dichloropyridin-4-yl)piperidine-4-carboxamide E13 (20 mg, 0.060 mmol) in MeOH (2 mL) was added benzaldehyde (19 μL, 0.19 mmol). After stirring for 45 min, sodium cyanoborohydride (12 mg, 0.19 mmol) was added and the mixture was stirred for a further 16 h. The solvent was removed under reduced pressure, the residue was dissolved in EtOAc (20 mL), washed with a saturated solution of sodium hydrogencarbonate (25 mL), brine (25 mL), dried (MgSO4) and the solvent was removed under reduced pressure. The crude product was purified by preparative tlc on silica gel (CH2Cl2, MeOH, 9:1) to furnish the title compound as a white solid (14 mg, 54%), m.p. 147-149° C.; umax (CHCl3)/cm−1 3007, 2837, 1658, 1558, 1509, 1457, 1146; m/z (ESI) C27H31Cl2N4O requires 497.1869, found [M+H]+ 497.1872.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08778925B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-68acebd68e70468290d6f31bfb763f20 |
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| Source note | uspto-grants-2014_07 |
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