HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622344Generated: October 31, 2026
4-Methoxybenzaldehyde → HCID 45275023, compound
https://huagongshe.com/reaction/1622344
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 45275021 | HCID 45275021 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 45275023 | HCID 45275023 | 19% |
Reaction Steps
To a solution of N-(2-aminoethyl)-1-(3,5-dichloropyridin-4-yl)piperidine-4-carboxamide E13 (50 mg, 0.16 mmol) in MeOH (5 mL) was added anisaldehyde (19 μL, 0.16 mmol). After stirring for 2 h, sodium cyanoborohydride (20 mg, 0.32 mmol) was added and the mixture was stirred for a further 20 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 colourless oil (13 mg, 19%), umax (CHCl3)/cm−1 3008, 2839, 1660, 1513, 1249, 1174, 1036; m/z (ESI) C21H27Cl2N4O2 requires 437.1506, found [M+H]+ 437.1508.
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-db0d5f9b229740e3a57a68ff96f332f6 |
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| Source note | uspto-grants-2014_07 |
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