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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386612Generated: November 1, 2026

2-Naphthalenecarboxaldehyde → HCID 59581353, compound

https://huagongshe.com/reaction/386612

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NaphthalenecarboxaldehydeHCID 6201—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59581287HCID 59581287—
SolventMethanolHCID 887—
ProductHCID 59581353HCID 59581353—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372859B2
Source datasetuspto-grants-2013_02
ORD IDord-d8dd2045ec68499f8c578e7f59466d76
Source noteuspto-grants-2013_02