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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598324Generated: October 31, 2026

Ethoxyacetyl chloride → 1-{[3-Amino-6-(benzyloxy)quinolin-4-yl]amino}-2-methylpropan-2-ol

https://huagongshe.com/reaction/598324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthoxyacetyl chlorideHCID 84189—
Reactant7-(Benzyloxy)-4-chloro-3-nitroquinolineHCID 21075751—
Reactant1-{[3-Amino-6-(benzyloxy)quinolin-4-yl]amino}-2-methylpropan-2-olHCID 67050945—
Reactant6-(Benzyloxy)-4-chloro-3-nitroquinolineHCID 67050992—
SolventAcetonitrileHCID 6342—
Product1-{[3-Amino-6-(benzyloxy)quinolin-4-yl]amino}-2-methylpropan-2-olHCID 67050945—
ProductN-{6-benzyloxy-4-[(2-hydroxy-2-methylpropyl)amino]quinolin-3-yl}-2-ethoxyacetamide hydrochlorideHCID 67051090—

Reaction Steps

1-{[3-Amino-6-(benzyloxy)quinolin-4-yl]amino}-2-methylpropan-2-ol was prepared according to the general methods described in Parts A and B of Example 54 using 6-benzyloxy-4-chloro-3-nitroquinoline in lieu of 7-benzyloxy-4-chloro-3-nitroquinoline in Part A. Ethoxyacetyl chloride (5.37 g, 43.8 mmol) was added to a solution of 1-{[3-amino-6-(benzyloxy)quinoline-4-yl]amino}-2-methylpropan-2-ol (7.45 g, 22.1 mmol) in acetonitrile (230 mL), and the reaction was stirred overnight. The solvent was removed under reduced pressure, and the residue was dissolved in dichloromethane. The resulting solution was washed with aqueous sodium bicarbonate, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography on a HORIZON HPFC system (an automated, modular high-performance flash purification product available from Biotage, Inc, Charlottesville, Va., USA) (silica gel cartridge, eluting with dichloromethane:methanol ranging in ratios from 98:2 to 95:5) to provide N-{6-benzyloxy-4-[(2-hydroxy-2-methylpropyl)amino]quinolin-3-yl}-2-ethoxyacetamide hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897597B2
Source datasetuspto-grants-2011_03
ORD IDord-24b3996053e545b7bb1679cd9e134c88
Source noteuspto-grants-2011_03