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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Amino-2-hydroxybutyric acid, (S)-(-)- | HCID 2733929 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Methyl 1-cyano-4-hydroxy-7-phenoxyisoquinoline-3-carboxylate | HCID 89812860 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | HCID 89812850 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409892B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-ccbb387a99cc44d2b5a372e92128c192 |
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| Source note | uspto-grants-2016_08 |
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