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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010427Generated: November 1, 2026

Diethylamine → HCID 11685165, compound

https://huagongshe.com/reaction/1010427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
ReactantPotassium CarbonateHCID 11430—
ReactantGlycidyl tosylate, (R)-HCID 154187—
ReactantHCID 135829386HCID 135829386—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuran ethyl acetateHCID 21939870—
ProductHCID 11685165HCID 1168516545.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

After adding (2R)oxiran-2-ylmethyl 4-methyl-1-benzenesulfonate (103 mg, 0.499 mmol), potassium carbonate (50 mg, 0.359 mmol) and dimethylformamide (3 ml) to N6-methyl-4-(3-chloro-4-(((methylamino)carbonyl)amino)phenoxy)-7-hydroxy-6-quinolinecarboxamide (120 mg, 0.299 mmol), the mixture was stirred at 60° C. for 7 hours. Next, diethylamine (1.5 ml) was added and the mixture was further stirred overnight at 60° C. The reaction solution was distributed between ethyl acetate-tetrahydrofuran (1:1) and water, and the organic layer was washed with water and saturated brine and then dried over anhydrous sodium sulfate. The solvent was distilled off, the residue was subjected to silica gel column chromatography (eluent—ethyl acetate:methanol=95:5), the fraction containing the target substance was concentrated, and crystals were precipitated from ethyl acetate-hexane (1:1), filtered out and blow-dried to obtain the title compound (71.8 mg, 0.135 mmol, 45.2%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973160B2
Source datasetuspto-grants-2011_07
ORD IDord-fde9e807c96e42d2b6ae8f2641fc08cc
Source noteuspto-grants-2011_07