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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387670Generated: October 30, 2026

Sodium Hydroxide → 7-(2-Oxazolyl)-1-oxo-2-(1-propylbutyl)-1,2,3,4-tetrahydroisoquinoline-5-carboxylic acid

https://huagongshe.com/reaction/387670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 68472426HCID 68472426—
Solvent1,4-DioxaneHCID 31275—
Product7-(2-Oxazolyl)-1-oxo-2-(1-propylbutyl)-1,2,3,4-tetrahydroisoquinoline-5-carboxylic acidHCID 6846969793.9%

Reaction Steps

320 mg of methyl 7-(2-oxazolyl]-1-oxo-2-(1-propylbutyl)-1,2,3,4-tetrahydroisoquinoline-5-carboxylate are dissolved in 7 cm3 of dioxane at a temperature close to 20° C. 2.1 cm3 of a 1N aqueous solution of sodium hydroxide are added, then the reaction mixture is heated at a temperature close to 60° C. for 30 min. The dioxane contained in the reaction mixture is concentrated to dryness under reduced pressure (5 kPa). 2.5 cm3 of a 1N aqueous solution of hydrochloric acid, 20 cm3 of dichloromethane and 20 cm3 of water are added to the residue obtained. After decanting, the organic phase is dried over anhydrous magnesium sulfate, filtered and concentrated to dryness under reduced pressure (5 kPa). 289 mg of 7-(2-oxazolyl]-1-oxo-2-(1-propylbutyl)-1,2,3,4-tetrahydroisoquinoline-5-carboxylic acid are obtained in the form of a beige powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372864B2
Source datasetuspto-grants-2013_02
ORD IDord-01fb23fbfef34a3d9a2584a3405dd423
Source noteuspto-grants-2013_02