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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023181Generated: October 26, 2026

N-(3,4-Dichlorophenyl)thiourea → 6-((2-(3,4-dichlorophenylamino)thiazol-4-yl)methoxy)-3,4-dihydroquinolin-2(1H)-one

https://huagongshe.com/reaction/1023181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3,4-Dichlorophenyl)thioureaHCID 710776—
Reactant6-(3-bromo-2-oxopropoxy)-3,4-dihydroquinolin-2(1H)-oneHCID 86680425—
SolventEthanolHCID 702—
Product6-((2-(3,4-dichlorophenylamino)thiazol-4-yl)methoxy)-3,4-dihydroquinolin-2(1H)-oneHCID 7154204124%

Reaction Steps

To a stirred solution of 6-(3-bromo-2-oxopropoxy)-3,4-dihydroquinolin-2(1H)-one (0.15 g, 0.503 mmol) in ethanol (3 mL) was added 1-(3,4-dichlorophenyl)thiourea (0.133 g, 0.604 mmol). The reaction mixture was refluxed for 12 h, then concentrated and purified by preparative HPLC to afford a white solid (0.05 g, 24%). 1H NMR 400 MHz, DMSO-d6: δ 2.40 (t, J=7.20 Hz, 2H), 2.85 (t, J=8.00 Hz, 2H), 4.99 (s, 2H), 6.80 (d, J=8.80 Hz, 1H), 6.87 (q, J=2.80 Hz, 1H), 6.92 (d, J=2.40 Hz, 1H), 6.98 (s, 1H), 7.48-7.49 (m, 2H), 8.06 (d, J=2.00 Hz, 1H), 9.92 (s, 1H), 10.56 (s, 1H). LCMS: RT 1.99 min; LCMS (ES-API), m/z 420. LCMS: RT 1.99 min; LCMS (ES-API), m/z 420.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722670B2
Source datasetuspto-grants-2014_05
ORD IDord-fa80333a63c44c39a55fd6c2daedc10c
Source noteuspto-grants-2014_05