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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481039Generated: October 30, 2026

4-Amino-2-hydroxybutyric acid, (S)-(-)- → HCID 89812850, compound

https://huagongshe.com/reaction/1481039

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-2-hydroxybutyric acid, (S)-(-)-HCID 2733929—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 1-cyano-4-hydroxy-7-phenoxyisoquinoline-3-carboxylateHCID 89812860—
Solvent2-MethoxyethanolHCID 8019—
ProductHCID 89812850HCID 89812850—

Reaction Steps

Methyl 1-cyano-4-hydroxy-7-phenoxyisoquinoline-3-carboxylate (200 mg, 0.63 mmol), (S)-4-amino-2-hydroxybutanoic acid (372 mg, 3.13 mmol, Sigma-Aldrich) and sodium methoxide (155 mg, 2.87 mmol) were suspended in 2-methoxyethanol (7 mL). The resulting mixture was heated to reflux for 3 hours and then cooled to room temperature. The solvent was removed in vacuo and the residue was dissolved in H2O (20 mL) and EtOAc (20 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 (0-20% MeOH/CH2Cl2 with 0.5% formic acid) to give the title compound in 180 mg. MS: (−) m/z 406.28 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409892B2
Source datasetuspto-grants-2016_08
ORD IDord-ccbb387a99cc44d2b5a372e92128c192
Source noteuspto-grants-2016_08