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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481146Generated: November 1, 2026

5-Aminovaleric acid → 5-{[4-Hydroxy-7-(4-methoxy-benzylamino)-isoquinoline-3-carbonyl]amino}-pentanoic acid

https://huagongshe.com/reaction/1481146

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Aminovaleric acidHCID 138—
ReactantMethanolHCID 887—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 4-hydroxy-7-(4-methoxybenzylamino)isoquinoline-3-carboxylateHCID 89813034—
Product5-{[4-Hydroxy-7-(4-methoxy-benzylamino)-isoquinoline-3-carbonyl]amino}-pentanoic acidHCID 89812999—

Reaction Steps

A mixture of methyl 4-hydroxy-7-(4-methoxybenzylamino)isoquinoline-3-carboxylate (21.0 mg, 0.06 mmol), 5-aminovaleric acid (269.3 mg, 2.3 mmol, Sigma-Aldrich) and NaOMe in MeOH (3.0 mL, 1.5 mmol, 0.5 M solution, Sigma-Aldrich) was heated to reflux for 20 hours before cooling to room temperature. The solvent was removed in vacuo and the residue was dissolved in H2O (10 mL) and EtOAc (10 mL). To the stirred mixture was added 1 N hydrochloric acid until pH was 1. The layers were separated and the aqueous layer was extracted twice with EtOAc. The combined organic layers were dried over MgSO4, concentrated, and purified by flash chromatography (0-30% MeOH/CH2Cl2) to give the title compound in 14 mg. MS: (−) m/z 422.13 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409892B2
Source datasetuspto-grants-2016_08
ORD IDord-e19e678c3bd84f858db8a5c2aec68733
Source noteuspto-grants-2016_08