HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399113Generated: October 27, 2026
Phenylacetaldehyde → HCID 70274489, compound
https://huagongshe.com/reaction/399113
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetaldehyde | HCID 998 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 70274442 | HCID 70274442 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 70274489 | HCID 70274489 | — |
Reaction Steps
cis-3-Methoxycarbonyl-5-[N-(1-(4-cyanobenzyl)-1H-imidazol-5-ylethyl)carbamoyl]piperidine (59.0 mg, 0.149 mmol) was dissolved in MeOH (2 mL). Phenylacetaldehyde (52.3 ul, 0.447 mmol) was added followed by sodium cyanoborohydride (28.1 mg, 0.447 mmol). The solution was stirred overnight at ambient temperature. The MeOH was removed under reduced pressure and chromatography (silica gel, 1-2% MeOH/CH2Cl2 /NH4OH) gave the title compound as a white solid. 1H NMR (CDCl3); δ7.62 (d, 2H, J=8 Hz), 7.50 (s, 1H), 7.08-7.37 (m, 7H), 6.88 (s, 1H), 6.46 (br s, 1H), 5.22 (s, 2H), 3.64 (s, 3H), 3.27-3.19 (m, 1H), 3.03-3.20 (m, 1H), 2.86-3.00 (m, 1H),2.73-2.85 (m, 3H), 2.44-2.70 (m, 5H), 2.26-2.41 (m, 2H), 1.98-2.10 (m, 2H), 1.80-1.95 (m, 1H). FAB MS 500 (M+1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05817678 |
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| Source dataset | uspto-grants-1998_10 |
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| ORD ID | ord-38d03fa451034cb4a5c8de38fc08c2fa |
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| Source note | uspto-grants-1998_10 |
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