HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386612Generated: November 1, 2026
2-Naphthalenecarboxaldehyde → HCID 59581353, compound
https://huagongshe.com/reaction/386612
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Naphthalenecarboxaldehyde | HCID 6201 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 59581287 | HCID 59581287 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 59581353 | HCID 59581353 | — |
Reaction Steps
A stirred solution of 2-amino-N-[(4S)-3-methyl-2,5-dioxo-1′,3′-dihydrospiro[imidazolidine-4,2′-inden]-5′-yl]acetamide from Step B (80.0 mg, 0.277 mmol) and 2-naphthaldehyde (65.0 mg, 0.416 mmol), in MeOH (3 mL) was heated to 50° C. After 5 hours, no additional formation of the intermediate imine could be observed, so the reaction was cooled to 0° C., prior to the introduction of sodium borohydride (21.0 mg, 0.555 mmol). After 10 minutes the reaction was complete. The bulk of the solvent was remove in vacuo, and the resulting residue was applied to a silica gel column for purification, eluting with DCM:MeOH (10% conc. NH4OH)—98:2 to 92:8. Product containing fractions were pooled and concentrated in vacuo to give the title compound. MS: m/z=429 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372859B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-d8dd2045ec68499f8c578e7f59466d76 |
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| Source note | uspto-grants-2013_02 |
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