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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481028Generated: October 25, 2026

(3R)-3-amino-3-phenylpropanoic acid → (R)-3-[(1-Cyano-4-hydroxy-7-phenoxy-isoquinoline-3-carbonyl)-amino]-3-phenyl-propionic acid

https://huagongshe.com/reaction/1481028

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3R)-3-amino-3-phenylpropanoic acidHCID 686703—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 89812860HCID 89812860—
Solvent2-MethoxyethanolHCID 8019—
Product(R)-3-[(1-Cyano-4-hydroxy-7-phenoxy-isoquinoline-3-carbonyl)-amino]-3-phenyl-propionic acidHCID 71737525—

Reaction Steps

Methyl 1-cyano-4-hydroxy-7-phenoxyisoquinoline-3-carboxylate (20 mg, 0.06 mmol), (R)-3-amino-3-phenyl-propionic acid (62 mg, 0.38 mmol, PepTech) and sodium methoxide (19 mg, 0.35 mmol) were suspended in 2-methoxyethanol (3 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 (15 mL) and EtOAc (15 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 (0-50% EtOAc/CH2Cl2 with 0.5% formic acid) to give the title compound in 17 mg. MS: (−) m/z 451.93 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409892B2
Source datasetuspto-grants-2016_08
ORD IDord-11613c29fc154c42b7661b7bd0258354
Source noteuspto-grants-2016_08