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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620232Generated: October 30, 2026

Isopropylamine → 2-(Isopropylamino)-6-methoxyquinoline-3-carbaldehyde

https://huagongshe.com/reaction/1620232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropylamineHCID 6363—
Reactant2-Chloro-6-methoxyquinoline-3-carbaldehydeHCID 689079—
SolventTetrahydrofuranHCID 8028—
Product2-(Isopropylamino)-6-methoxyquinoline-3-carbaldehydeHCID 8666982099.2%

Reaction Conditions

Temperature180 °C

Reaction Steps

To a stirred solution of 2-chloro-6-methoxyquinoline-3-carbaldehyde (1.50 g, 6.77 mmol) in THF (10 mL) in a 20 mL microwave vial equipped with a magnetic stirrer was added propan-2-amine (5.76 mL, 67.7 mmol) and the reaction mixture was stirred for 12.5 h at 160° C. and finally 45 min at 180° 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. The volatiles were then removed at 40° C. under vacuum and the residue was then neutralised with a saturated NaHCO3 aqueous solution before extraction with CH2Cl2 (100 mL). The organic layer was washed with brine (20 mL), dried over MgSO4, filtered, and concentrated under vacuum to give 2-(isopropylamino)-6-methoxyquinoline-3-carbaldehyde SLA 28186 as an orange solid (1.64 g, 99% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772316B2
Source datasetuspto-grants-2014_07
ORD IDord-c1885b70b7e5438fa4ebd0560a1d6e71
Source noteuspto-grants-2014_07