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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167233Generated: October 30, 2026

1-Naphthaldehyde → HCID 136247054, compound

https://huagongshe.com/reaction/2167233

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphthaldehydeHCID 6195—
Reactant2-Amino-5-methoxybenzamideHCID 20338217—
ProductHCID 136247054HCID 136247054—

Reaction Steps

Compound 17 was synthesized from 5-methoxy-2-aminobenzamide (9) (1.2 g, 7.3 mmol) and 1-naphthaldehyde (14) (1.1 g, 7.3 mmol): yield 1.5 g (70%); pale yellow needles; mp 174 to 175° C.; 1H NMR (DMSO-d6) δ 3.87 (3H, s, OCH3), 7.22-7.34 (2H, m, 2×ArH), 7.53-7.72 (5H, m, 5×ArH), 7.95-8.22 (3H, m, 3×ArH), 12.62 (1H, br s, NH) ppm; MS (ESI) m/z 302; Anal. (C19H14N2O2): C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045437B2
Source datasetuspto-grants-2015_06
ORD IDord-d1e0da8f75664a5aaf31485f52e61236
Source noteuspto-grants-2015_06