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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1629678Generated: November 2, 2026

Water → HCID 66625363, compound

https://huagongshe.com/reaction/1629678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBis(2-bromoethyl) etherHCID 21521—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 66625187HCID 66625187—
SolventTolueneHCID 1140—
ProductHCID 66625363HCID 6662536375.7%

Reaction Steps

(Step 6) 66.1 mg of ethyl (2S,4S)-1-acetyl-4-(4-aminophenoxy)-2-methyl-1,2,3,4-tetrahydroquinoline-6-carboxylate was dissolved in 2 mL of toluene, and 312 μL of N,N-diisopropylethylamine and 113 μL of 2-bromoethyl ether were added to the solution at 0° C. The mixture was heated to reflux for 14 hours. After completion of the reaction, the reaction liquid was cooled, water was added thereto, and the mixture was extracted three times with chloroform. The extraction product was washed with saturated brine, dehydrated over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by using silica gel chromatography (hexane:ethyl acetate=1:1), and thus 59.4 mg (75.7%) of ethyl (2S,4S)-1-acetyl-2-methyl-4-(4-morpholinophenoxy)-1,2,3,4-tetrahydroquinoline-6-carboxylate was obtained as a pale yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791090B2
Source datasetuspto-grants-2014_07
ORD IDord-b1ccaf7f5d964c7e9a96255c9afcce4d
Source noteuspto-grants-2014_07