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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494179Generated: October 31, 2026

Potassium Carbonate → 1-(2-Morpholin-4-ylethyl)-7-nitro-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/494179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant7-Nitro-1,2,3,4-tetrahydroquinolineHCID 252513—
Reactant4-(2-iodoethyl)morpholineHCID 11149168—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-(2-Morpholin-4-ylethyl)-7-nitro-1,2,3,4-tetrahydroquinolineHCID 588741187.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 7-nitro-1,2,3,4-tetrahydroquinoline (D1) (246 mg, 1.38 mmol) in DMF (2.7 ml) was added potassium carbonate (574 mg, 4.15 mmol) followed by a solution of 4-(2-iodoethyl)morpholine (500 mg, 2.07 mmol) in DMF (2 ml) and the reaction heated to 70° C. After cooling to ambient temperature the reaction mixture was diluted with water and extracted with EtOAc which was washed with water, dried over MgSO4 and concentrated in vacuo to give the crude product which was purified by silica SPE chromatography. Elution with 80% EtOAc/petroleum ether gave the title compound as an orange gum (29 mg). 1H NMR (250 MHz, CDCl3) δ (ppm): 7.39 (m, 2H), 7.00 (d, 1H), 3.73 (m, 4H), 3.47 (m, 2H), 3.38 (m, 2H), 2.79 (t, 2H), 2.49-2.59 (m, 6H), 1.96 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538121B2
Source datasetuspto-grants-2009_05
ORD IDord-c1f11253054c41899e4cbefe6415ca3c
Source noteuspto-grants-2009_05