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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050884Generated: November 2, 2026

2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline → HCID 89508724, compound

https://huagongshe.com/reaction/1050884

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinolineHCID 27833—
ReactantHCID 71553880HCID 71553880—
ReactantHCID 89501167HCID 89501167—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 89508724HCID 8950872438%

Reaction Steps

A flame-dried flask was charged with maleimidocaproyl-valine-alanine linker (Compound 36 of Example 13 in WO 2011/130613 A1) (11 mg, 29 μmol, 1.5 eq) dissolved in 0.8 mL of 5% methanol in anhydrous dichloromethane. The acid was pre-activated by addition of N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (9 mg, 34 μmol, 1.8 eq), followed by stirring at room temperature under nitrogen for 15 minutes. The activated acid was then added to a flame-dried flask containing PBD dimer 14 (13 mg, 19 μmol, 1 eq). The reaction was stirred for 4 hours at room temperature under nitrogen, at which time LC-MS revealed conversion to product. The material was diluted in dichloromethane and purified by radial chromatography on a 1 mm chromatotron plate eluted with CH2Cl2/MeOH mixtures (100:0 to 80:20) to provide 15 (7.7 mg, 38%). LC-MS: m/z (ES+) found 1075.5 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09387259B2
Source datasetuspto-grants-2016_07
ORD IDord-7e403174449243a9a21f22079acb257e
Source noteuspto-grants-2016_07