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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44772Generated: October 28, 2026

Triethylamine → N-(2-chloro-4-{[(4-hydroxytetrahydro-2H thiopyran-4-yl)methyl]amino}quinolin-3-yl)butanamide

https://huagongshe.com/reaction/44772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantButyryl chlorideHCID 8855—
Reactant4-{[(3-Amino-2-chloroquinolin-4-yl)amino]methyl}tetrahydro-2h-thiopyran-4-olHCID 87204871—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductN-(2-chloro-4-{[(4-hydroxytetrahydro-2H thiopyran-4-yl)methyl]amino}quinolin-3-yl)butanamideHCID 87204895—

Reaction Steps

Under a nitrogen atmosphere butyryl chloride (322 μL, 3.11 mmol) was added dropwise was added to a suspension of 4-{[(3-amino-2-chloroquinolin-4-yl)amino]methyl}tetrahydro-2H-thiopyran-4-ol (0.92 g, 2.83 mmol) in dichloromethane (28 mL). After 2 hours triethylamine (0.79 mL, 5.66 mol) was added and the reaction mixture was stirred for 2 hours. More butyryl chloride (0.2 mL) and triethylamine (0.30 mL) were added. The reaction mixture was stirred for an additional hour and then diluted with saturated aqueous sodium bicarbonate (50 mL) and extracted with dichloromethane (3×60 mL). The combined organics were washed with saturated aqueous sodium bicarbonate (40 mL) and brine (30 mL), dried over sodium sulfate, filtered, and then concentrated under reduced pressure to provide N-(2-chloro-4-{[(4-hydroxytetrahydro-2H thiopyran-4-yl)methyl]amino}quinolin-3-yl)butanamide as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541438B2
Source datasetuspto-grants-2013_09
ORD IDord-525eebb8562b4025b9c1e18ed3a2615e
Source noteuspto-grants-2013_09