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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882695Generated: October 31, 2026

6-Aminoquinoline → Z-Val-Pro 6-aminoquinoline

https://huagongshe.com/reaction/882695

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-AminoquinolineHCID 11373—
ReactantDiisopropylcarbodiimideHCID 12734—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantZ-Val-pro-OHHCID 10783923—
SolventDichloromethaneHCID 6344—
ProductZ-Val-Pro 6-aminoquinolineHCID 131729872—

Reaction Steps

A solution of Z-Val-Pro-OH (217.4 mg, 0.62 mmol) in dichloromethane (1.5 mL), was successively treated at room temperature. with 1-hydroxibenzotriazol (84.3 mg, 0.62 mmol), N,N′-diisopropylcarbodiimide (97.2 μL, 0.62 mmol) and 6-aminoquinoline (75 mg, 0.52 mmol). The stirring was continued until the complete disappearance of the starting material (overnight). Then, the solvent was evaporated, the residue was dissolved in ethyl acetate and washed with citric acid (10%), NaHCO3 (10%) and brine. The organic layer was dried (Na2SO4) and evaporated leaving a residue that was purified by CCTLC on the chromatotron with hexane/ethyl acetate (1:4) to yield H (20 yield

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236756B2
Source datasetuspto-grants-2012_08
ORD IDord-837f8df55324406d983aa5ce7878dffa
Source noteuspto-grants-2012_08