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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715069Generated: October 31, 2026

Ethyl Acetate → HCID 58840906, compound

https://huagongshe.com/reaction/1715069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant6-AminoquinolineHCID 11373—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantHCID 68637473HCID 68637473—
SolventAcetonitrileHCID 6342—
ProductHCID 58840906HCID 58840906—

Reaction Steps

(7S)-7-Benzyloxycarbonylamino-octanedioic acid 8-tert-butyl ester (10.0 g, 26.3 mmol), 6-aminoquinoline (4.02 g, 27.9 mmol) and EDCI (6.07 g, 29.0 mmol) were dissolved in 150 mL anhydrous CH3CN. The solution was stirred at RT for 2 h. The solvent was removed under reduced pressure, and the residue was dissolved in 500 mL EtOAc and washed with 1 M HCl (200×3) and water (100×2). The organic layer was dried over anhydrous Na2SO4 Removal of solvent gave 16 g crude product. The pure compound 9.0 g was obtained with column separation (ethyl acetate as eluent) in 68% as a thick oil. 1H NMR (CDCl3) δ 8.80 (1H, d), 8.70 (1H, s), 8.30 (1H, d), 8.00 (2H, t), 7.56-7.20 (7H), 5.40 (1H, d), 5.08 (2H, s), 4.38 (1H, m), 2.20 (2H, t), 2.0-1.6 (17H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799803B2
Source datasetuspto-grants-2010_09
ORD IDord-a80a72affb284ca4b6ace57bc8b8e4c6
Source noteuspto-grants-2010_09