Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495470Generated: October 31, 2026

Toluene → N-tert-butyloxycarbonyl-6-methoxy-3-aminoquinoline

https://huagongshe.com/reaction/495470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactanttert-ButanolHCID 6386—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant6-Methoxy-3-carboxyaminoquinolineHCID 22326813—
SolventEthyl AcetateHCID 8857—
ProductN-tert-butyloxycarbonyl-6-methoxy-3-aminoquinolineHCID 22326880—

Reaction Steps

To a stirred suspension of 6-methoxy-3-carboxyaminoquinoline (Step E, 4.8 g, 0.021 mol) in toluene (109 mL) was added DPPA (5.83 mL, 0.026 mol) followed by TEA (3.6 mL, 0.026 mol). The reaction was stirred at RT for 30 min. t-BuOH (8.22 mL, 0.086 mL) was added then the mixture was heated at reflux for 8 h. The solution was diluted with EtOAc and washed 2× with a saturated solution of NH4Cl and 2× with water. The EtOAc solution was dried over MgSO4 and evaporated. The mixture was purified by flash chromatography using 20% EtOAc/hexane to give N-tert-butyloxycarbonyl-6-methoxy-3-aminoquinoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939874B2
Source datasetuspto-grants-2005_09
ORD IDord-c4c6315a29a34643a09a809c1788a9a0
Source noteuspto-grants-2005_09