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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336198Generated: October 30, 2026

2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline → (S)-1-(1,1-Dioxo-1lambda6-thiomorpholine-4-carbonyl)-piperidine-2-carboxylic acid (5-ethyl-4-phenyl-thiazol-2-yl)-amide

https://huagongshe.com/reaction/336198

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinolineHCID 27833—
Reactant2-Thiazolamine, 5-ethyl-4-phenyl-HCID 147560—
Reactant(2S)-1-[(1,1-Dioxido-4-thiomorpholinyl)carbonyl]-2-piperidinecarboxylic acidHCID 58563809—
SolventDichloromethaneHCID 6344—
Product(S)-1-(1,1-Dioxo-1lambda6-thiomorpholine-4-carbonyl)-piperidine-2-carboxylic acid (5-ethyl-4-phenyl-thiazol-2-yl)-amideHCID 46873413—

Reaction Steps

To a solution of (S)-1-(1,1-Dioxo-1λ6-thiomorpholine-4-carbonyl)-piperidine-2-carboxylic acid (92 mg; 0.317 mmol) and 2-amino-5-ethyl-4-phenyl-1,3-thiazole (64.8 mg; 0.317 mmol) in dichloromethane (4 mL) is added 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline (79.1 mg; 0.32 mmol). The reaction mixture is left stirring at room temperature for 18 hours. The reaction mixture is directly purified by preparative HPLC provides the title compound, m/z 477 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889670B2
Source datasetuspto-grants-2014_11
ORD IDord-0bc276f75f5949db9988b07030642a86
Source noteuspto-grants-2014_11