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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620196Generated: October 25, 2026

Methylamine → 6-Methoxy-2-(methylamino)quinoline-3-carbaldehyde

https://huagongshe.com/reaction/1620196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant2-Chloro-6-methoxyquinoline-3-carbaldehydeHCID 689079—
Solvent1,4-DioxaneHCID 31275—
Product6-Methoxy-2-(methylamino)quinoline-3-carbaldehydeHCID 8666981698.4%

Reaction Conditions

Temperature160 °C

Reaction Steps

To a stirred solution of 2-chloro-6-methoxyquinoline-3-carbaldehyde (1.50 g, 6.77 mmol) in 1,4-dioxan (10 mL) in a 20 mL microwave vial equipped with a magnetic stirrer was added methylamine (40 wt % solution in water, 2.10 mL, 24.3 mmol) and the reaction mixture was stirred for 6 h at 160° C. under microwave irradiation. After cooling to RT, the volatiles were removed at 40° C. under vacuum and the resulting yellow oil was taken up in a mixture of THF:1 N aq. HCl=1:1 (50 mL) and stirred for 1 h at RT. THF was removed at 40° C. under vacuum and the residue was then neutralised with a saturated NaHCO3 aqueous solution before to be extracted with CH2Cl2 (100 mL). The organic phase was washed with brine (20 mL), dried over MgSO4, filtered, and concentrated under vacuum, to give 6-methoxy-2-(methylamino)quinoline-3-carbaldehyde SLA 28150 as an orange oil (1.44 g, 98% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772316B2
Source datasetuspto-grants-2014_07
ORD IDord-0f3fb6519888473c9e09461f52d15de5
Source noteuspto-grants-2014_07