Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266843Generated: November 2, 2026

2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline → (2S,4S)-4-acetylthio-1-allyloxycarbonyl-2-(3-allyloxycarbonylphenylcarbamoyl)pyrrolidine

https://huagongshe.com/reaction/266843

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinolineHCID 27833—
Reactant(2S,4S)-4-Acetylthio-1-allyloxycarbonyl-2-carboxypyrrolidineHCID 15299255—
ReactantAllyl 3-aminobenzoateHCID 18930599—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product(2S,4S)-4-acetylthio-1-allyloxycarbonyl-2-(3-allyloxycarbonylphenylcarbamoyl)pyrrolidineHCID 53680604101.1%

Reaction Steps

(2S,4S)-4-Acetylthio-1-allyloxycarbonyl-2-carboxypyrrolidine (2.54 g, 9.3 mM), allyl 3-aminobenzoate (1.5 g, 8.5 mM), and 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline (2.72 g, 11 mM) were dissolved in toluene (50 ml) and stirred for 18 hours at ambient temperature. The reaction mixture was diluted with ethyl acetate (150 ml) and washed with 2H HCl (3 by 30 ml), water, saturated NaHCO3, and brine. Drying over HgSO4 and evaporation gave (2S,4S)-4-acetylthio-1-allyloxycarbonyl-2-(3-allyloxycarbonylphenylcarbamoyl)pyrrolidine as a gum (3.7 g, 100%) in a state sufficiently pure for further work. Nmr (CDCl3): δ 2.32 (s, 3H); 2.60 (br, 2H); 3.40 (dd, 1H); 4.03 (quintet, 1H); 4.13 (dd, 1H); 4.57 (t, 1H); 4.66 (dm, 2H); 4.82 (dt, 2H); 5.23-5.46 (m, 4H); 5.86-6.12 (m, 2H); 7.41 (t, 1H); 7.82 (d, 1H); 7.91 (d, 1H); 8.07 (t, 1H); 9.18 (br, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652233
Source datasetuspto-grants-1997_07
ORD IDord-c7e16562c5994a288e6759112891a4e8
Source noteuspto-grants-1997_07