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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489287Generated: October 29, 2026

Hydrochloric Acid → HCID 23587792, compound

https://huagongshe.com/reaction/489287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhenethylamineHCID 1001—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 22266516HCID 22266516—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
ProductHCID 23587792HCID 2358779274.7%

Reaction Steps

1-Butyl-2-oxo-1,2,5,6,7,8-hexahydroquinoline-3-carboxylic acid (4-002-01) (100 mg, 0.38 mmol) was dissloved in toluene (10 mL), and to the reaction mixture were added thionyl chloride (83 μL, 1.14 mmol) and catalytic amount of DMF, and the reaction mixture was reacted at 75° C. for 30 min. The reaction mixture was evaporated under reduced pressure and the residue was dissolved in methylene chloride (5 mL). To the reaction mixture was added phenethylamine (143 μL, 1.14 mmol) and the reaction mixture was stirred at room temperature for 10 min. To the reaction mixture was added diluted hydrochloric acid (1 mol/L, 10 mL) and the reaction mixture was extracted with ethyl acetate (30 mL), washed with brine (10 mL), dried over anhydrous magnesium sulfate, and evaporated under reduced pressure. The residue was purified by silica gel column chromatography (toluene/ethyl acetate), followed by recrystallization from diethyl ether to give 1-butyl-2-oxo-1,2,5,6,7,8-hexahydroquinoline-3-carboxylic acid phenethylamide (4-002) (100 mg, 74%) as white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06977266B2
Source datasetuspto-grants-2005_12
ORD IDord-4ea82e1471904a76880db0372eb0e6c1
Source noteuspto-grants-2005_12