Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060430Generated: October 29, 2026

Methanol → 2-(S)-{[7-(4-Fluoro-phenoxy)-4-hydroxy-isoquinoline-3-carbonyl]-amino}-propionic acid

https://huagongshe.com/reaction/2060430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantL-AlanineHCID 5950—
Reactant7-(4-Fluoro-phenoxy)-4-hydroxy-isoquinoline-3-carboxylic acid butyl esterHCID 66712966—
ReactantHCID 178418582HCID 178418582—
Product2-(S)-{[7-(4-Fluoro-phenoxy)-4-hydroxy-isoquinoline-3-carbonyl]-amino}-propionic acidHCID 5747336949.6%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 7-(4-fluoro-phenoxy)-4-hydroxy-isoquinoline-3-carboxylic acid butyl ester (154 mg, 0.43 mmol), (S)-alanine (225 mg, 2.5 mmol) and a 0.5 N solution of MeONa in MeOH (5 ml, 2.5 mmol) was heated in a microwave oven with stirring for 20 min at 130° C. before the mixture was concentrated in vacuo. To the residue was added water (15 ml) and the mixture was washed with Et2O (3×30 ml). The purified aq. solution was acidified by the addition of 6 N HCl and extracted with EtOAc (1×30 ml). The organic phase was dried over MgSO4 and concentrated in vacuo to give the title compound as a tan solid (79 mg); MS-(−)-ion M−1=369.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278325B2
Source datasetuspto-grants-2012_10
ORD IDord-a30136319e1e49f58cd484193084ddef
Source noteuspto-grants-2012_10