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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728549Generated: October 29, 2026

3-Butyryl-4-chloro-8-methoxyquinoline → HCID 14989684, compound

https://huagongshe.com/reaction/728549

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Butyryl-4-chloro-8-methoxyquinolineHCID 11777567—
Reactant3-Methylthiophen-2-amineHCID 14536436—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 14989684HCID 1498968436.4%

Reaction Steps

3-Butyryl-4-chloro-8-methoxyquinoline (3.6 g, 0.0137 mol) and 2-amino-3-methylthiophene (3.4 g, 0.03 mol) in 1,4 dioxan (30 ml) under a nitrogen atmosphere were stirred at room temperature for 20 hours. The solvent was evaporated under reduced pressure to give an oil. The oil was taken up in dichloromethane and extracted with 2N hydrochloric acid (3×100ml). The dichloromethane extracts were then washed with sodium carbonate solution (100 ml), dried over magnesium sulphate, filtered and evaporated under reduced pressure to give a solid. The solid was purified by flash chromatography using a gradient elution of dichloromethane/methanol (0-5%, 500 ml). The fractions containing the product were combined and evaporated under reduced pressure to give a solid, (1.94 g), m.p. 130°-132°. Recrystallization from ethyl acetate gave the title compound, (1.7 g), m.p. 132°-133°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05049567
Source datasetuspto-grants-1991_09
ORD IDord-d6b2990135504790a9e44904127027a7
Source noteuspto-grants-1991_09