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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22600Generated: October 28, 2026

Acetic Acid → 5-(3-(2-(7-Chloroquinolin-2-YL)ethyl)phenyl)-8-dimethylcarbamyl-4,6-dithiaoctanoic acid

https://huagongshe.com/reaction/22600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethylamineHCID 674—
Reactant2-Chloro-1-methylpyridinium iodideHCID 167069—
ReactantHCID 10413257HCID 10413257—
SolventTolueneHCID 1140—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product5-(3-(2-(7-Chloroquinolin-2-YL)ethyl)phenyl)-8-dimethylcarbamyl-4,6-dithiaoctanoic acidHCID 19930521—

Reaction Steps

To a suspension of diacid (Example 25) (0.3 g) in dichloromethane (20 mL), acetonitrile (5 mL) and triethylamine (200 μL) was added 2-chloro-1-methylpyridinium iodide (180 mg). The mixture was stirred 30 min, cooled to 0° and 0.32 mL of a 2M solution of dimethylamine in toluene was added. The reaction was stirred 2 hours at room temperature. The reaction mixture was poured onto NH4OAc buffer and acetic acid (5 mL) was added. The mixture was extracted with ethyl acetate, which was dried over sodium sulfate and evaporated. Purification of the residue by flash chromatography starting with 15% and finishing with 30% of THF in toluene containing 1% of acetic acid afforded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428171
Source datasetuspto-grants-1995_06
ORD IDord-6a7ee6954ddc497abbbbcc193478656f
Source noteuspto-grants-1995_06